Canonical Allele Identifier: PA1139689399
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 918818
ClinVar RCV Id: RCV001176648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ala48Pro
CA346734921
NM_001281492.2:c.142G>C