Canonical Allele Identifier: PA096674
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30925
ClinVar RCV Id: RCV000023913 RCV000059709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Gly338Arg
CA026494
NM_080669.6:c.1012G>C