Canonical Allele Identifier: PA916071286
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 653395
ClinVar RCV Id: RCV000809163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Phe96Leu
CA402996310
NM_138924.3:c.288C>A
CA402996319
NM_138924.3:c.288C>G
CA402996343
NM_138924.3:c.286T>C