Canonical Allele Identifier: PA2826956843
Gene: GNPAT HGNC NCBI

Linked Data

ClinVar Variation Id: 161670
ClinVar RCV Id: RCV000149206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303279.1:p.Lys584Asn
CA174569
NM_001316350.2:c.1752G>C
CA345240356
NM_001316350.2:c.1752G>T