Canonical Allele Identifier: PA2826635755
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1058037
ClinVar RCV Id: RCV001367126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Glu405Ala
CA346750984
NM_001281494.2:c.1214A>C