Canonical Allele Identifier: PA2826625107
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455355
ClinVar RCV Id: RCV000550227 RCV002376987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Val164Asp
CA346740670
NM_001281492.2:c.491T>A