Canonical Allele Identifier: PA2826297824
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30923
ClinVar RCV Id: RCV000023911 RCV000059708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Ala335Asp
CA026493
NM_001242366.3:c.1004C>A