Canonical Allele Identifier: PA096696
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 853

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Ser318Arg
CA026509
NM_080669.6:c.954C>G
CA398346906
NM_080669.6:c.954C>A
CA398346934
NM_080669.6:c.952A>C