Canonical Allele Identifier: PA2825234735
Gene: AGL HGNC NCBI

Linked Data

ClinVar Variation Id: 377192
ClinVar RCV Id: RCV000425245 RCV001083855 RCV003912603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000637.2:p.Thr1461Ser
CA967437
NM_000646.2:c.4382C>G
CA341342567
NM_000646.2:c.4381A>T