Canonical Allele Identifier: PA2828722379
Gene: GPHN HGNC NCBI

Linked Data

ClinVar Variation Id: 466209
ClinVar RCV Id: RCV000548955 RCV002526142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364448.1:p.Ala91Thr
CA7233704
NM_001377519.1:c.271G>A