Canonical Allele Identifier: PA2579910560
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1003806
ClinVar RCV Id: RCV001300411
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ala111Ser
CA346730006
NM_000251.3:c.331G>T