Canonical Allele Identifier: PA2825971345
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2160131
ClinVar RCV Id: RCV003075793

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Pro327Ser
CA382897129
NM_001164277.2:c.979C>T