Canonical Allele Identifier: PA190704
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 184990
ClinVar RCV Id: RCV000164341 RCV000469980 RCV001775642 RCV002228583 RCV003995335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg248Gln
CA016402
NM_000179.3:c.743G>A