Canonical Allele Identifier: PA2825972092
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557269
ClinVar RCV Id: RCV000673387
ClinVar Variation Id: 991008
ClinVar RCV Id: RCV001279137 RCV002480908
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Val162Leu
CA6311753
NM_001164279.2:c.484G>T
CA6311754
NM_001164279.2:c.484G>C