Canonical Allele Identifier: PA645294405
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181495
ClinVar RCV Id: RCV000159044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Phe71Val
CA297073
NM_080601.3:c.211T>G