Canonical Allele Identifier: PA2826297851
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 21743
ClinVar RCV Id: RCV000020948 RCV000059712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Pro397Arg
CA026498
NM_001242366.3:c.1190C>G