Canonical Allele Identifier: PA645390677
Gene: GNPTAB HGNC NCBI

Linked Data

ClinVar Variation Id: 388282
ClinVar RCV Id: RCV000421294 RCV001114040 RCV001114039 RCV002059848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077288.2:p.Val781Met
CA6746445
NM_024312.5:c.2341G>A