Canonical Allele Identifier: PA916056447
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40499
ClinVar RCV Id: RCV000033470 RCV000151689 RCV000586528 RCV000686123 RCV003150933 RCV004532486
ClinVar Variation Id: 477670
ClinVar RCV Id: RCV000534502 RCV000593077
ClinVar Variation Id: 2582571
ClinVar RCV Id: RCV003333581 RCV003333582 RCV003333580
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Phe71Leu
CA273215
NM_080601.3:c.211T>C
CA386777846
NM_080601.3:c.213T>A
CA386777847
NM_080601.3:c.213T>G