Canonical Allele Identifier: PA2826628742
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 234648
ClinVar RCV Id: RCV000219779 RCV001526277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Thr1091Arg
CA10577290
NM_001281492.2:c.3272C>G