Canonical Allele Identifier: PA645387982
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 361383
ClinVar RCV Id: RCV000328391 RCV000659097 RCV003922617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Gly380Arg
CA4625299
NM_178857.5:c.1138G>A
CA370296249
NM_178857.5:c.1138G>C