Canonical Allele Identifier: PA2825972271
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472481
ClinVar RCV Id: RCV001969292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Ala300Gly
CA6311629
NM_001164279.2:c.899C>G