Canonical Allele Identifier: PA645509925
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 439188
ClinVar RCV Id: RCV000508402 RCV001865650 RCV003159641 RCV004003547
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Met672Val
CA033352
NM_000251.3:c.2014A>G