Canonical Allele Identifier: PA2825068387
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2446453
ClinVar RCV Id: RCV003159287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Asn92Asp
CA402996427
NM_000156.6:c.274A>G