Canonical Allele Identifier: PA096643
Gene: SLC46A1 HGNC NCBI
ClinVar Allele:
15893
ClinVar RCV:
RCV000000902
RCV000059710
ClinVar Variation:
854
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Arg376Trp
CA026496
NM_080669.6:c.1126C>T