Canonical Allele Identifier: PA2826637290
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142270
ClinVar RCV Id: RCV000131293 RCV000234661 RCV001560125 RCV003398768 RCV003998098
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Tyr764Cys
CA011852
NM_001281494.2:c.2291A>G