Canonical Allele Identifier: PA2826631899
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89291
ClinVar RCV Id: RCV000222631 RCV000524146 RCV000479488 RCV000662498 RCV000759136 RCV003137607 RCV003997079 RCV004542741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys564Thr
CA010469
NM_001281493.2:c.1691A>C