Canonical Allele Identifier: PA1139672993
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 858947
ClinVar RCV Id: RCV001064940 RCV001250339 RCV001530275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Trp25Cys
CA3808667
NM_000322.5:c.75G>C
CA364138821
NM_000322.5:c.75G>T