Allele Registry

Canonical Allele Identifier: PA2741809367

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV003277953

ClinVar Variation:

2556001

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gln385Lys	CA68181110 NM_000030.3:c.1153C>A