Canonical Allele Identifier: PA2499230099
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023370
ClinVar RCV Id: RCV001323400 RCV002412037
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val63Ala
CA346729020
NM_000251.3:c.188T>C