Canonical Allele Identifier: PA2825972196
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2722187
ClinVar RCV Id: RCV003508479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Arg246Leu
CA6311680
NM_001164279.2:c.737G>T