Canonical Allele Identifier: PA645471991
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421880
ClinVar RCV Id: RCV000484112 RCV000566386 RCV001053129 RCV004003363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys249Thr
CA16617563
NM_000251.3:c.746A>C