Canonical Allele Identifier: PA2499231089
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1175289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Asp194Glu
CA364135887
NM_000322.5:c.582T>G
CA364135889
NM_000322.5:c.582T>A