Canonical Allele Identifier: PA658832694
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551427
ClinVar RCV Id: RCV000666485
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Tyr8His
CA6311933
NM_001164277.2:c.22T>C