Canonical Allele Identifier: PA2826630976
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195062
ClinVar RCV Id: RCV001557993 RCV002414265 RCV003759061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly348Asp
CA346750527
NM_001281493.2:c.1043G>A