Canonical Allele Identifier: PA096611
Gene: SLC46A1 HGNC NCBI
ClinVar Allele:
15894
ClinVar RCV:
RCV000000903
RCV000059714
ClinVar Variation:
855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Arg113Cys
CA026506
NM_080669.6:c.337C>T