Canonical Allele Identifier: PA2828721155
Gene: GPHN HGNC NCBI

Linked Data

ClinVar Variation Id: 466209
ClinVar RCV Id: RCV000548955 RCV002526142
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364445.1:p.Ala91Thr
CA7233704
NM_001377516.1:c.271G>A