Canonical Allele Identifier: PA2825007523
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 556204
ClinVar RCV Id: RCV000672173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Tyr1489del
CA341342640
NM_000028.2:c.4467T>A
CA341342641
NM_000028.2:c.4467T>G
CA658821101
NM_000028.2:c.4465_4467del