Canonical Allele Identifier: PA2825068238
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1368103
ClinVar RCV Id: RCV001874331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Phe10Leu
CA402998422
NM_000156.6:c.30C>G
CA402998423
NM_000156.6:c.30C>A
CA402998430
NM_000156.6:c.28T>C