Canonical Allele Identifier: PA2826633898
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1040426
ClinVar RCV Id: RCV001344067 RCV002377458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Arg1002Met
CA346761442
NM_001281493.2:c.3005G>T