Canonical Allele Identifier: PA2826631322
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479867
ClinVar RCV Id: RCV000564228 RCV000688061 RCV000765685 RCV001591322 RCV004000868 RCV003470823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Lys426Arg
CA068575
NM_001281493.2:c.1277A>G