Canonical Allele Identifier: PA915953997
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663797
ClinVar RCV Id: RCV000821748 RCV002408984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Asp603Ala
CA346728332
NM_000251.3:c.1808A>C