Canonical Allele Identifier: PA2825065099
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 646375
ClinVar RCV Id: RCV000800653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000143.2:p.Met172Val
CA401361724
NM_000152.5:c.514A>G