Canonical Allele Identifier: PA658801628
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 524213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Trp47Cys
CA413937041
NM_000169.3:c.141G>T
CA413937045
NM_000169.3:c.141G>C