Canonical Allele Identifier: PA2825068293
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1448647
ClinVar RCV Id: RCV002002298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Pro40Ser
CA304067305
NM_000156.6:c.118C>T