Canonical Allele Identifier: PA2825068314
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2097117
ClinVar RCV Id: RCV003016531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Ala52Ser
CA402998048
NM_000156.6:c.154G>T