Allele Registry

Canonical Allele Identifier: PA273898

Gene: AGXT HGNC NCBI

ClinVar Allele:

186656

ClinVar RCV:

RCV000169046

RCV001066143

ClinVar Variation:

188738

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Gly161Cys	CA273897 NM_000030.3:c.481G>T