Canonical Allele Identifier: PA645426160
Gene: SLC25A13 HGNC NCBI

Linked Data

ClinVar Variation Id: 252921
ClinVar RCV Id: RCV000239389 RCV000595565 RCV001163201 RCV002057271 RCV003475850 RCV003909878
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055066.1:p.Pro502Leu
CA4352889
NM_014251.3:c.1505C>T