Canonical Allele Identifier: PA239060
Gene: RP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 193521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_976033.1:p.Ala12Thr
CA239059
NM_203288.2:c.34G>A