Canonical Allele Identifier: PA2573167109
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1497792
ClinVar RCV Id: RCV001996263
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Met138Leu
CA364137617
NM_000322.5:c.412A>C
CA364137618
NM_000322.5:c.412A>T