Canonical Allele Identifier: PA314795
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205575
ClinVar RCV Id: RCV000187558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala3Ser
CA314794
NM_000156.6:c.7G>T