Canonical Allele Identifier: PA2826629595
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823445

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gln23Glu
CA346740972
NM_001281493.2:c.67C>G