Canonical Allele Identifier: PA916011488
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483799
ClinVar RCV Id: RCV000566943 RCV000586719 RCV000813407 RCV004001055 RCV002483532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu984Gln
CA346758738
NM_001281492.2:c.2951T>A