Canonical Allele Identifier: PA645390590
Gene: GNPTAB HGNC NCBI

Linked Data

ClinVar Variation Id: 397560
ClinVar RCV Id: RCV000449579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077288.2:p.Asp534Asn
CA6746584
NM_024312.5:c.1600G>A