Canonical Allele Identifier: PA2825007273
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1010037
ClinVar RCV Id: RCV001307610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Asp1261Glu
CA967213
NM_000028.2:c.3783T>G
CA341337830
NM_000028.2:c.3783T>A