Canonical Allele Identifier: PA2826464977
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 573580
ClinVar RCV Id: RCV000695286 RCV003478422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Lys595Arg
CA346728877
NM_001258281.1:c.1784A>G