Canonical Allele Identifier: PA915967721
Gene: AMPH HGNC NCBI

Linked Data

ClinVar Variation Id: 711336
ClinVar RCV Id: RCV000883077
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001626.1:p.Thr586Met
CA4225393
NM_001635.4:c.1757C>T