Canonical Allele Identifier: PA2826635201
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89219
ClinVar RCV Id: RCV000131189 RCV000485534 RCV000524119 RCV001818236 RCV002498356 RCV003466936 RCV004019093
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser278Leu
CA009108
NM_001281494.2:c.833C>T