Canonical Allele Identifier: PA1139705426
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 861812
ClinVar RCV Id: RCV001068407 RCV002497473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Leu182Phe
CA6311813
NM_001467.6:c.544C>T