Canonical Allele Identifier: PA2573300686
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462338
ClinVar RCV Id: RCV001985667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Ala13Pro
CA398354942
NM_080669.6:c.37G>C