Canonical Allele Identifier: PA2826297757
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 322409
ClinVar RCV Id: RCV000385629 RCV001317868 RCV003993930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Val171Asp
CA8458319
NM_001242366.3:c.512T>A