Canonical Allele Identifier: PA2573300021
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1415000
ClinVar RCV Id: RCV001930755

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ile9Asn
CA402998441
NM_138924.3:c.26T>A