Canonical Allele Identifier: PA658810671
Gene: GNPTAB HGNC NCBI

Linked Data

ClinVar Variation Id: 522908
ClinVar RCV Id: RCV000626103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077288.2:p.Ala34Pro
CA386486903
NM_024312.5:c.100G>C