Allele Registry

Canonical Allele Identifier: PA093626

Gene: AMN HGNC NCBI

ClinVar RCV:

RCV000005036

RCV001851660

ClinVar Variation:

4770

HGVS (amino-acid)	Matching Registered Transcripts
NP_112205.2:p.Thr41Ile	CA117064 NM_030943.4:c.122C>T