Canonical Allele Identifier: PA2825006062
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1415807
ClinVar RCV Id: RCV001921087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Asn49Asp
CA966073
NM_000028.2:c.145A>G