Canonical Allele Identifier: PA127989
Gene: SLC25A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 18249
ClinVar RCV Id: RCV000019911 RCV000414338 RCV000626767 RCV000626768 RCV000626769 RCV001198599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001142.2:p.Ala123Asp
CA127988
NM_001151.4:c.368C>A