Canonical Allele Identifier: PA658828882
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13326
ClinVar RCV Id: RCV000014254 RCV000033516 RCV000077863 RCV000156977 RCV000621227 RCV000515324 RCV000576594 RCV000850589 RCV000999988 RCV001253546 RCV001270562 RCV001293867 RCV001813192 RCV003991568 RCV003147284 RCV004541002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asn308Asp
CA220158
NM_080601.3:c.922A>G