Allele Registry

Canonical Allele Identifier: PA2580515620

Gene: AMPH HGNC NCBI

ClinVar RCV:

RCV004140135

ClinVar Variation:

2293019

HGVS (amino-acid)	Matching Registered Transcripts
NP_647477.1:p.Ile8Val	CA367297525 NM_139316.3:c.22A>G