Canonical Allele Identifier: PA916071198
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205575
ClinVar RCV Id: RCV000187558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ala3Ser
CA314794
NM_138924.3:c.7G>T