Canonical Allele Identifier: PA658739851
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491820
ClinVar RCV Id: RCV000582667
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val891Gly
CA346731493
NM_000251.3:c.2672T>G