Canonical Allele Identifier: PA645475359
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428464
ClinVar RCV Id: RCV000490880 RCV000664310 RCV000659883 RCV001209603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly692Trp
CA346729189
NM_000251.3:c.2074G>T