Canonical Allele Identifier: PA2826633481
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483860
ClinVar RCV Id: RCV000561463 RCV003767182 RCV004001064
ClinVar Variation Id: 644019
ClinVar RCV Id: RCV000797853
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly922Arg
CA346760855
NM_001281493.2:c.2764G>A
CA346760859
NM_001281493.2:c.2764G>C