Allele Registry

Canonical Allele Identifier: PA2829336206

Gene: AMPH HGNC NCBI

ClinVar RCV:

RCV004151737

ClinVar Variation:

2299123

HGVS (amino-acid)	Matching Registered Transcripts
NP_001626.1:p.Pro305Thr	CA4225802 NM_001635.4:c.913C>A