Canonical Allele Identifier: PA1139689118
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 845501
ClinVar RCV Id: RCV001048576 RCV002436591
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ser9Asn
CA346734506
NM_001281492.2:c.26G>A