Allele Registry

Canonical Allele Identifier: PA2499271927

Gene: AASS HGNC NCBI

ClinVar RCV:

RCV001420630

ClinVar Variation:

1098670

HGVS (amino-acid)	Matching Registered Transcripts
NP_005754.2:p.Leu465Val	CA165925623 NM_005763.4:c.1393C>G