Canonical Allele Identifier: PA2825068479
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1387928
ClinVar RCV Id: RCV001884313

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.His145Gln
CA402995115
NM_000156.6:c.435C>G
CA402995116
NM_000156.6:c.435C>A