Canonical Allele Identifier: PA645387980
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 361384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Phe376Leu
CA4625303
NM_178857.5:c.1128C>G
CA370296285
NM_178857.5:c.1128C>A
CA370296295
NM_178857.5:c.1126T>C