Canonical Allele Identifier: PA2825971851
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2143661
ClinVar RCV Id: RCV003062770
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Met307Val
CA6311691
NM_001164278.2:c.919A>G