Canonical Allele Identifier: PA916010921
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 455330
ClinVar RCV Id: RCV000546866
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu17Pro
CA346734547
NM_001281492.2:c.50T>C