Canonical Allele Identifier: PA2826630608
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89217
ClinVar RCV Id: RCV000131251 RCV000212651 RCV000411714 RCV001080487 RCV001328467 RCV004542740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly264Arg
CA009071
NM_001281493.2:c.790G>A
CA346747544
NM_001281493.2:c.790G>C