Canonical Allele Identifier: PA2825006249
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2154319
ClinVar RCV Id: RCV003081725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Phe257Leu
CA27568743
NM_000028.2:c.771C>G
CA341339871
NM_000028.2:c.769T>C
CA341339886
NM_000028.2:c.771C>A