Canonical Allele Identifier: PA2825006069
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_000019.2:p.Phe62Leu
CA966080
NM_000028.2:c.186C>G
CA341329387
NM_000028.2:c.184T>C
CA341329394
NM_000028.2:c.186C>A