Allele Registry

Canonical Allele Identifier: PA274059

Gene: AGXT HGNC NCBI

ClinVar Allele:

186653

ClinVar RCV:

RCV000169219

RCV001850392

ClinVar Variation:

188866

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Leu101Pro	CA274058 NM_000030.3:c.302T>C