Allele Registry

Canonical Allele Identifier: PA091327

Gene: AGXT HGNC NCBI

ClinVar Allele:

20679

ClinVar RCV:

RCV000005994

RCV000420710

ClinVar Variation:

5640

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Ser205Pro	CA340441 NM_000030.3:c.613T>C