Canonical Allele Identifier: PA2826625215
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 485866
ClinVar RCV Id: RCV000566632 RCV001858374
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Glu188Lys
CA346740840
NM_001281492.2:c.562G>A