Canonical Allele Identifier: PA2825972173
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557363
ClinVar RCV Id: RCV000673495
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Gly229Ser
CA382897946
NM_001164279.2:c.685G>A