Canonical Allele Identifier: PA2741884941
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2722187
ClinVar RCV Id: RCV003508479

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Arg319Leu
CA6311680
NM_001467.6:c.956G>T