Canonical Allele Identifier: PA2826633365
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001075
ClinVar RCV Id: RCV001297305 RCV001531315 RCV002451659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ala896Thr
CA346760536
NM_001281493.2:c.2686G>A