Canonical Allele Identifier: PA2580263025
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2182999
ClinVar RCV Id: RCV002611137
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.His301Tyr
CA229597212
NM_001467.6:c.901C>T