Canonical Allele Identifier: PA891865617
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 592136
ClinVar RCV Id: RCV000723338
ClinVar Variation Id: 2723215
ClinVar RCV Id: RCV003518436
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000633.2:p.Thr38Ser
CA341329061
NM_000642.3:c.112A>T
CA341329065
NM_000642.3:c.113C>G