Canonical Allele Identifier: PA913192000
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 593549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.[Asp55Val;Gln57Leu]
CA913190392
NM_000169.3:c.164_171delinsTCTGCCTA
CA2695235012
NM_000169.3:c.164_170delinsTCTGCCT