Canonical Allele Identifier: PA095173
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91104
ClinVar RCV Id: RCV000076607 RCV000490837
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val161Asp
CA021196
NM_000251.3:c.482T>A