Canonical Allele Identifier: PA645470882
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237357
ClinVar RCV Id: RCV000227770 RCV000480195 RCV000563870 RCV002465579 RCV003469135 RCV003998750
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gln4Lys
CA10581987
NM_000251.3:c.10C>A