Canonical Allele Identifier: PA2580114014
Gene: PRPH2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2476427
ClinVar RCV Id: RCV003198404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000313.2:p.Lys47Asn
CA364138686
NM_000322.5:c.141G>T
CA364138687
NM_000322.5:c.141G>C