Allele Registry

Canonical Allele Identifier: PA2741905031

Gene: AGPS HGNC NCBI

ClinVar Allele:

2711883

ClinVar RCV:

RCV003291879

ClinVar Variation:

2538945

HGVS (amino-acid)	Matching Registered Transcripts
NP_003650.1:p.Ser65Leu	CA349700794 NM_003659.4:c.194C>T