Canonical Allele Identifier: PA2573309269
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352767
ClinVar RCV Id: RCV002049541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Met160Leu
CA370300043
NM_178857.5:c.478A>T
CA370300045
NM_178857.5:c.478A>C