Canonical Allele Identifier: PA2825068225
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2192764
ClinVar RCV Id: RCV002607645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro4Ser
CA304067374
NM_000156.6:c.10C>T