Canonical Allele Identifier: PA2826297815
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 853
ClinVar RCV Id: RCV000000901 RCV000059717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Ser318Arg
CA026509
NM_001242366.3:c.954C>G
CA398346906
NM_001242366.3:c.954C>A
CA398346934
NM_001242366.3:c.952A>C