Allele Registry

Canonical Allele Identifier: PA2580515624

Gene: AMPH HGNC NCBI

ClinVar RCV:

RCV004151737

ClinVar Variation:

2299123

HGVS (amino-acid)	Matching Registered Transcripts
NP_647477.1:p.Pro305Thr	CA4225802 NM_139316.3:c.913C>A