Canonical Allele Identifier: PA2826625998
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774324
ClinVar RCV Id: RCV002392326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Asp376Asn
CA346746337
NM_001281492.2:c.1126G>A