Canonical Allele Identifier: PA2741884939
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3021350
ClinVar RCV Id: RCV003872493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Met315Arg
CA382897483
NM_001467.6:c.944T>G