Canonical Allele Identifier: PA2573309257
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Thr150Ala
CA4625695
NM_178857.5:c.448A>G