Canonical Allele Identifier: PA2827261914
Gene: SLC6A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613343
ClinVar RCV Id: RCV003362292

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001315559.1:p.Leu386Phe
CA340067666
NM_001328630.2:c.1156C>T