Canonical Allele Identifier: PA2825006051
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 592136
ClinVar RCV Id: RCV000723338
ClinVar Variation Id: 2723215
ClinVar RCV Id: RCV003518436

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000019.2:p.Thr38Ser
CA341329061
NM_000028.2:c.112A>T
CA341329065
NM_000028.2:c.113C>G