Canonical Allele Identifier: PA2829984766
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 3163613
ClinVar RCV Id: RCV004456430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068380.3:p.Gly297Val
CA8760867
NM_021734.5:c.890G>T