Canonical Allele Identifier: PA645474986
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 231656
ClinVar RCV Id: RCV000219670 RCV001240753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp654Glu
CA10577991
NM_000251.3:c.1962C>G
CA346728800
NM_000251.3:c.1962C>A