Canonical Allele Identifier: PA2826626404
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568709
ClinVar RCV Id: RCV000689151 RCV002397384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gly469Ala
CA346749323
NM_001281492.2:c.1406G>C