Canonical Allele Identifier: PA645382061
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 229774
ClinVar RCV Id: RCV000219569 RCV000470330 RCV002282050 RCV003997769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg791His
CA068883
NM_000179.3:c.2372G>A