Canonical Allele Identifier: PA2499301808
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297704
ClinVar RCV Id: RCV001723469

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Thr198Ala
CA370299710
NM_178857.5:c.592A>G