Canonical Allele Identifier: PA645476385
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 408472
ClinVar RCV Id: RCV002230359 RCV003298485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Lys912Gln
CA16611064
NM_000251.3:c.2734A>C