Canonical Allele Identifier: PA2573249728
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478280
ClinVar RCV Id: RCV001998569

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Asn1392Ser
CA4751812
NM_006269.2:c.4175A>G