Canonical Allele Identifier: PA105978
Gene: SLC25A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 18248
ClinVar RCV Id: RCV000019910
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001142.2:p.Asp104Gly
CA127987
NM_001151.4:c.311A>G