Canonical Allele Identifier: PA2825972188
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3021350
ClinVar RCV Id: RCV003872493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Met242Arg
CA382897483
NM_001164279.2:c.725T>G