Canonical Allele Identifier: PA096632
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65749
ClinVar RCV Id: RCV000055980 RCV000059711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Arg376Gln
CA026497
NM_080669.6:c.1127G>A