Canonical Allele Identifier: PA2825972651
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 578167
ClinVar RCV Id: RCV000701095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Lys212del
CA6311763
NM_001164280.2:c.634_636del