Canonical Allele Identifier: PA2825084963
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_000170.1:p.Ser14Thr
CA346734532
NM_000179.3:c.40T>A