Canonical Allele Identifier: PA2827312756
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40496
ClinVar RCV Id: RCV000687319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp61Val
CA282073
NM_001330437.2:c.182A>T