Canonical Allele Identifier: PA2825230658
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 1470739
ClinVar RCV Id: RCV001964324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Phe41Leu
CA966077
NM_000646.2:c.121T>C
CA341329329
NM_000646.2:c.123T>G
CA341329330
NM_000646.2:c.123T>A