Canonical Allele Identifier: PA645436868
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 374339
ClinVar RCV Id: RCV000415279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Trp1451Cys
CA967423
NM_000642.3:c.4353G>T
CA341342402
NM_000642.3:c.4353G>C