Canonical Allele Identifier: PA193197
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185867
ClinVar RCV Id: RCV000165367 RCV000482477 RCV000630080 RCV001262375 RCV003995412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Tyr1298Cys
CA014634
NM_000179.3:c.3893A>G