Canonical Allele Identifier: PA096688
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 21743
ClinVar RCV Id: RCV000020948 RCV000059712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Pro425Arg
CA026498
NM_080669.6:c.1274C>G