Canonical Allele Identifier: PA2830278260
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_647477.1:p.Thr544Met
CA4225393
NM_139316.3:c.1631C>T