ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827608352
Gene: RPS29
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
150452
ClinVar RCV:
RCV000128851
ClinVar Variation:
140739
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001338304.1:p.Ile47Thr
CA163479
NM_001351375.2:c.140T>C