Canonical Allele Identifier: PA219290
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68271
ClinVar RCV Id: RCV000059121
ClinVar Variation Id: 2678969
ClinVar RCV Id: RCV003472945
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Gly50Arg
CA219288
NM_001164277.2:c.148G>C
CA382907843
NM_001164277.2:c.148G>A