Canonical Allele Identifier: PA916056469
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13340
ClinVar RCV Id: RCV000014268 RCV000033480 RCV000037641 RCV000157680 RCV000515381 RCV000590740 RCV001813202 RCV002453257 RCV004532344
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Gln79Arg
CA235322
NM_080601.3:c.236A>G