Canonical Allele Identifier: PA2573217949
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1484818
ClinVar RCV Id: RCV002008199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Leu251Val
CA382901003
NM_001467.6:c.751C>G