Canonical Allele Identifier: PA645390761
Gene: GNPTAB HGNC NCBI

Linked Data

ClinVar Variation Id: 306802
ClinVar RCV Id: RCV000322774 RCV000880925 RCV000376997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_077288.2:p.Glu968Asp
CA6746323
NM_024312.5:c.2904A>C
CA386296103
NM_024312.5:c.2904A>T