Canonical Allele Identifier: PA2826626433
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 925229
ClinVar RCV Id: RCV001187057 RCV001223021 RCV003469305 RCV004008659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Lys476Glu
CA346749421
NM_001281492.2:c.1426A>G