Canonical Allele Identifier: PA2826633864
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185867
ClinVar RCV Id: RCV000165367 RCV000482477 RCV000630080 RCV001262375 RCV003995412
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Tyr996Cys
CA014634
NM_001281493.2:c.2987A>G