Canonical Allele Identifier: PA2826634566
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 127559
ClinVar RCV Id: RCV000115373 RCV000218965
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly128Arg
CA008438
NM_001281494.2:c.382G>A
CA346744165
NM_001281494.2:c.382G>C