Allele Registry

Canonical Allele Identifier: PA122789

Gene: SLC6A4 HGNC NCBI

ClinVar RCV:

RCV000013798

RCV001127236

ClinVar Variation:

12935

HGVS (amino-acid)	Matching Registered Transcripts
NP_001036.1:p.Ile425Val	CA122788 NM_001045.6:c.1273A>G