Allele Registry

Canonical Allele Identifier: PA2829336177

Gene: AMPH HGNC NCBI

ClinVar RCV:

RCV004140135

ClinVar Variation:

2293019

HGVS (amino-acid)	Matching Registered Transcripts
NP_001626.1:p.Ile8Val	CA367297525 NM_001635.4:c.22A>G