Canonical Allele Identifier: PA645471584
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408460
ClinVar RCV Id: RCV000568213 RCV000458857 RCV000759835 RCV003449128 RCV004000775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Val147Ile
CA038750
NM_000251.3:c.439G>A