Canonical Allele Identifier: PA2828722336
Gene: GPHN HGNC NCBI

Linked Data

ClinVar Variation Id: 1995840
ClinVar RCV Id: RCV002819410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364448.1:p.Gln14His
CA390255108
NM_001377519.1:c.42A>C
CA390255109
NM_001377519.1:c.42A>T