Canonical Allele Identifier: PA913202268
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13327
ClinVar RCV Id: RCV000014255 RCV000037669 RCV000033518 RCV000157682 RCV000588570 RCV000515421 RCV001027696 RCV001197417 RCV001813193 RCV004532339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn308Ser
CA235328
NM_080601.3:c.923A>G