Canonical Allele Identifier: PA658671064
Gene: GPHN HGNC NCBI

Linked Data

ClinVar Variation Id: 466209

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065857.1:p.Ala91Thr
CA7233704
NM_020806.5:c.271G>A