Canonical Allele Identifier: PA2580114018
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2101438
ClinVar RCV Id: RCV003033746

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Asp50Asn
CA3808657
NM_000322.5:c.148G>A