Canonical Allele Identifier: PA331631
Gene: MSH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 91135
ClinVar RCV Id: RCV000076639 RCV000822250 RCV002345387 RCV003452951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000242.1:p.Leu187Arg
CA021414
NM_000251.3:c.560T>G