Canonical Allele Identifier: PA2580336849
Gene: RP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2131955
ClinVar RCV Id: RCV003055912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006260.1:p.Thr1435Ala
CA177181668
NM_006269.2:c.4303A>G