Canonical Allele Identifier: PA2825972547
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 552538
ClinVar RCV Id: RCV000667820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157752.1:p.Phe134Leu
CA382903967
NM_001164280.2:c.402T>G
CA382903974
NM_001164280.2:c.402T>A
CA382903995
NM_001164280.2:c.400T>C