Canonical Allele Identifier: PA2826636181
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790981
ClinVar RCV Id: RCV002450382 RCV003759734
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu505Gln
CA069001
NM_001281494.2:c.1513G>C