Canonical Allele Identifier: PA915964604
Gene: GAA HGNC NCBI

Linked Data

ClinVar Variation Id: 281299
ClinVar Variation Id: 325787
ClinVar RCV Id: RCV000398587
ClinVar Variation Id: 2062189
ClinVar RCV Id: RCV002953248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073272.1:p.Met440Ile
CA8815260
NM_001079804.3:c.1320G>T
CA10650363
NM_001079804.3:c.1320G>C
CA401365421
NM_001079804.3:c.1320G>A