Canonical Allele Identifier: PA916010968
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 818296
ClinVar RCV Id: RCV001009768 RCV001862757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala35Thr
CA346734836
NM_001281492.2:c.103G>A