Canonical Allele Identifier: PA913201564
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 623352
ClinVar RCV Id: RCV000761499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Leu251Pro
CA382900995
NM_001164277.2:c.752T>C