Canonical Allele Identifier: PA2826297719
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 855
ClinVar RCV Id: RCV000000903 RCV000059714
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Arg113Cys
CA026506
NM_001242366.3:c.337C>T