Canonical Allele Identifier: PA2579921919
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2453482
ClinVar RCV Id: RCV003182937
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.His785Asp
CA346729973
NM_000251.3:c.2353C>G