Canonical Allele Identifier: PA915988194
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 215176
ClinVar RCV Id: RCV000200213 RCV001833153 RCV002492905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Met72Val
CA324773
NM_001164279.2:c.214A>G