Canonical Allele Identifier: PA2573300028
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1368103
ClinVar RCV Id: RCV001874331

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Phe10Leu
CA402998422
NM_138924.3:c.30C>G
CA402998423
NM_138924.3:c.30C>A
CA402998430
NM_138924.3:c.28T>C