Canonical Allele Identifier: PA645475230
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231326
ClinVar RCV Id: RCV000221435 RCV002228960 RCV003462461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Tyr678His
CA10577996
NM_000251.3:c.2032T>C