Canonical Allele Identifier: PA2580123035
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 2100818
ClinVar RCV Id: RCV003014600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Phe991Leu
CA341326063
NM_000646.2:c.2971T>C
CA341326069
NM_000646.2:c.2973T>A
CA341326076
NM_000646.2:c.2973T>G