Canonical Allele Identifier: PA334484
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 188269
ClinVar RCV Id: RCV000168249 RCV000220140 RCV000411795 RCV000759151 RCV000781571 RCV001355537 RCV003468827 RCV003995618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Arg178His
CA015812
NM_000179.3:c.533G>A