Canonical Allele Identifier: PA2580544089
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2475607
ClinVar RCV Id: RCV003208712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Ile407Met
CA370295941
NM_178857.5:c.1221C>G