Canonical Allele Identifier: PA2825972766
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557209
ClinVar RCV Id: RCV000673318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Met311Val
CA229597135
NM_001164280.2:c.931A>G