Canonical Allele Identifier: PA2825972200
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554872
ClinVar RCV Id: RCV000670580
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Val247Leu
CA382897325
NM_001164279.2:c.739G>T
CA382897333
NM_001164279.2:c.739G>C