ClinGen Allele Registry
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Canonical Allele Identifier:
PA915986102
Gene: SLC25A13
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000020699
RCV001378585
RCV001826486
RCV003473112
ClinVar Variation:
21509
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001153682.1:p.Gly532Asp
CA342150
NM_001160210.2:c.1595G>A