Canonical Allele Identifier: PA2826624755
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073252
ClinVar RCV Id: RCV004015266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu52Ala
CA346734950
NM_001281492.2:c.155A>C