Canonical Allele Identifier: PA658832787
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 550787
ClinVar RCV Id: RCV000665629
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Val333Leu
CA382896394
NM_001164277.2:c.997G>T
CA382896397
NM_001164277.2:c.997G>C