Canonical Allele Identifier: PA2825230662
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1045170
ClinVar RCV Id: RCV001349536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Phe46Leu
CA966080
NM_000646.2:c.138C>G
CA341329387
NM_000646.2:c.136T>C
CA341329394
NM_000646.2:c.138C>A