Canonical Allele Identifier: PA2826628399
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89383
ClinVar RCV Id: RCV000491285 RCV000545459 RCV001355496
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Gln1016Pro
CA012827
NM_001281492.2:c.3047A>C