Canonical Allele Identifier: PA2580114004
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2053126

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Val28Met
CA364138807
NM_000322.5:c.82G>A