Canonical Allele Identifier: PA658654602
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 444739
ClinVar RCV Id: RCV000513317 RCV000765984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Thr150Ile
CA370300127
NM_178857.5:c.449C>T