Canonical Allele Identifier: PA2825971319
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765207
ClinVar RCV Id: RCV002449880 RCV003100062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Asn298Lys
CA382898024
NM_001164277.2:c.894C>G
CA382898027
NM_001164277.2:c.894C>A