Canonical Allele Identifier: PA645475404
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231482
ClinVar RCV Id: RCV000221209 RCV000479697 RCV000553991 RCV003997901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Glu701Ala
CA10577998
NM_000251.3:c.2102A>C