Canonical Allele Identifier: PA2580510328
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2097117
ClinVar RCV Id: RCV003016531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Ala52Ser
CA402998048
NM_138924.3:c.154G>T