Canonical Allele Identifier: PA658738031
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 491765
ClinVar RCV Id: RCV000583346 RCV001860087 RCV004002329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Thr457Ala
CA346724787
NM_000251.3:c.1369A>G