Canonical Allele Identifier: PA658676467
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 450331
ClinVar RCV Id: RCV000521099 RCV000655370
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.His147Gln
CA402995066
NM_000156.6:c.441C>G
CA402995067
NM_000156.6:c.441C>A