Canonical Allele Identifier: PA2826624691
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1742543
ClinVar RCV Id: RCV002335306 RCV003102620 RCV004005671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala16Thr
CA346734539
NM_001281492.2:c.46G>A