Canonical Allele Identifier: PA658672963
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 483667
ClinVar RCV Id: RCV000561848 RCV001065224 RCV003987610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Ile747Val
CA346729739
NM_000251.3:c.2239A>G