Allele Registry

Canonical Allele Identifier: PA3057579409

Gene: ASPA HGNC NCBI

ClinVar RCV:

RCV004723854

ClinVar Variation:

3343501

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121557.1:p.Ala305Val	CA397688248 NM_001128085.1:c.914C>T