Canonical Allele Identifier: PA106942
Gene: PAX6 HGNC NCBI

Linked Data

ClinVar Variation Id: 372441

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000271.1:p.Arg208Trp
CA5933833
NM_000280.6:c.622C>T