Canonical Allele Identifier: PA2573165161
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356045
ClinVar RCV Id: RCV001880333
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu768Gly
CA346729860
NM_000251.3:c.2303A>G