Canonical Allele Identifier: PA2741884937
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3032086
ClinVar RCV Id: RCV003899820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Gly292Ala
CA382898187
NM_001467.6:c.875G>C