Canonical Allele Identifier: PA2826634262
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Lys15Glu
CA346740815
NM_001281494.2:c.43A>G