Canonical Allele Identifier: PA2826631517
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 957715
ClinVar RCV Id: RCV001230742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys473Gln
CA068824
NM_001281493.2:c.1417A>C