Canonical Allele Identifier: PA2825230631
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 848952
ClinVar RCV Id: RCV001052812
ClinVar Variation Id: 2071780

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Val30Leu
CA966071
NM_000646.2:c.88G>T
CA27560501
NM_000646.2:c.88G>C