Canonical Allele Identifier: PA2826297679
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Pro8Ser
CA026503
NM_001242366.3:c.22C>T