Canonical Allele Identifier: PA299315
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 182560
ClinVar RCV Id: RCV000160587 RCV000573867 RCV000821313 RCV003998471
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr495Ala
CA018401
NM_000251.3:c.1483A>G