Canonical Allele Identifier: PA129167
Gene: SIX3 HGNC NCBI

Linked Data

ClinVar Variation Id: 30381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005404.1:p.Gly37Cys
CA129166
NM_005413.4:c.109G>T