Canonical Allele Identifier: PA2826631559
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034588
ClinVar RCV Id: RCV001337331 RCV003462906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.His483Arg
CA346753556
NM_001281493.2:c.1448A>G