Canonical Allele Identifier: PA226308
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 98706
ClinVar RCV Id: RCV000085019 RCV000132580 RCV003114252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Trp246Arg
CA226307
NM_000322.5:c.736T>C
CA364135047
NM_000322.5:c.736T>A