Canonical Allele Identifier: PA645482014
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 328354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Thr7Asn
CA9043813
NM_000156.6:c.20C>A