Canonical Allele Identifier: PA658832764
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551070
ClinVar RCV Id: RCV000666035
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Ala268Val
CA229597856
NM_001164277.2:c.803C>T