Canonical Allele Identifier: PA2825459662
Gene: GAA HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073271.1:p.His56Leu
CA294886644
NM_001079803.3:c.167A>T