Canonical Allele Identifier: PA2499231055
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1063671
ClinVar RCV Id: RCV001373528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Met23Ile
CA3808669
NM_000322.5:c.69G>A
CA364138836
NM_000322.5:c.69G>T
CA364138837
NM_000322.5:c.69G>C