Canonical Allele Identifier: PA2573192069
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1507301
ClinVar RCV Id: RCV002013432 RCV002324478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Pro38Ala
CA346734854
NM_001281492.2:c.112C>G