Canonical Allele Identifier: PA916012124
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 232391
ClinVar RCV Id: RCV000222748 RCV001301937 RCV002267961
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly916Arg
CA10578153
NM_001281494.2:c.2746G>C