Canonical Allele Identifier: PA645474689
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 428463
ClinVar RCV Id: RCV000491233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Gly587Cys
CA346728239
NM_000251.3:c.1759G>T