Canonical Allele Identifier: PA916056431
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40496
ClinVar RCV Id: RCV000687319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asp61Val
CA282073
NM_080601.3:c.182A>T