Canonical Allele Identifier: PA2826624687
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1737846
ClinVar RCV Id: RCV002323336 RCV003126243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser14Thr
CA346734532
NM_001281492.2:c.40T>A