Canonical Allele Identifier: PA915963447
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 374339
ClinVar RCV Id: RCV000415279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000635.2:p.Trp1451Cys
CA967423
NM_000644.2:c.4353G>T
CA341342402
NM_000644.2:c.4353G>C