Canonical Allele Identifier: PA915988210
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 496949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Ser91Arg
CA6311826
NM_001164279.2:c.273C>A
CA382902943
NM_001164279.2:c.273C>G
CA382902974
NM_001164279.2:c.271A>C