Canonical Allele Identifier: PA2825972371
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551776
ClinVar RCV Id: RCV000666917
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Gly20Ala
CA382908699
NM_001164280.2:c.59G>C