Canonical Allele Identifier: PA1139762286
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 908814
ClinVar RCV Id: RCV001159501 RCV002070967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Arg85Trp
CA4625792
NM_178857.5:c.253C>T
CA645560803
NM_178857.5:c.252_253delinsTT