Canonical Allele Identifier: PA163480
Gene: RPS29 HGNC NCBI
ClinVar Allele:
150452
ClinVar RCV:
RCV000128851
ClinVar Variation:
140739
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025172.1:p.Ile50Thr
CA163479
NM_001030001.4:c.149T>C