Allele Registry

Canonical Allele Identifier: PA117882

Gene: RP1 HGNC NCBI

ClinVar RCV:

RCV000081369

RCV000337903

RCV001519927

RCV001794435

RCV001851697

RCV003887855

ClinVar Variation:

5969

HGVS (amino-acid)	Matching Registered Transcripts
NP_006260.1:p.Asn985Tyr	CA117881 NM_006269.2:c.2953A>T