Canonical Allele Identifier: PA916028151
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13332
ClinVar RCV Id: RCV000014260 RCV000033543 RCV000156995 RCV000212897 RCV001851849 RCV002490364 RCV004532342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Ser506Thr
CA180739
NM_001330437.2:c.1516T>A