Canonical Allele Identifier: PA2826624754
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2013606
ClinVar RCV Id: RCV002834790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu52Asp
CA346734952
NM_001281492.2:c.156G>C
CA346734953
NM_001281492.2:c.156G>T