Canonical Allele Identifier: PA2826956720
Gene: GNPAT HGNC NCBI

Linked Data

ClinVar Variation Id: 296120
ClinVar RCV Id: RCV000390788 RCV001511741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303279.1:p.Asn287Ser
CA1451947
NM_001316350.2:c.860A>G