Canonical Allele Identifier: PA1139689386
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 960208
ClinVar RCV Id: RCV001233688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser43Pro
CA346734883
NM_001281492.2:c.127T>C