Canonical Allele Identifier: PA916056420
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 179221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asp61Ala
CA273600
NM_080601.3:c.182A>C