Canonical Allele Identifier: PA2580543968
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2125973
ClinVar RCV Id: RCV003049841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Ser142Thr
CA370300208
NM_178857.5:c.424T>A