Canonical Allele Identifier: PA2826464649
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 90771
ClinVar RCV Id: RCV000076270 RCV000700587 RCV002408594 RCV003452855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001245210.1:p.Gly521Arg
CA019199
NM_001258281.1:c.1561G>C