Canonical Allele Identifier: PA2580456693
Gene: GNPTAB HGNC NCBI

Linked Data

ClinVar Variation Id: 2151371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077288.2:p.Phe3Leu
CA6747031
NM_024312.5:c.9C>G
CA386487094
NM_024312.5:c.9C>A
CA386487099
NM_024312.5:c.7T>C