Canonical Allele Identifier: PA2827608352
Gene: RPS29 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338304.1:p.Ile47Thr
CA163479
NM_001351375.2:c.140T>C