Canonical Allele Identifier: PA2825068395
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 653395
ClinVar RCV Id: RCV000809163
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Phe96Leu
CA402996310
NM_000156.6:c.288C>A
CA402996319
NM_000156.6:c.288C>G
CA402996343
NM_000156.6:c.286T>C