Canonical Allele Identifier: PA645426241
Gene: SLC25A19 HGNC NCBI

Linked Data

ClinVar Variation Id: 281113
ClinVar RCV Id: RCV000340152 RCV000388085 RCV000838506 RCV003930038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_068380.3:p.Met266Arg
CA8760877
NM_021734.5:c.797T>G