Canonical Allele Identifier: PA2580107312
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2137773
ClinVar RCV Id: RCV003058489 RCV004070147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Lys235Asn
CA9043527
NM_000156.6:c.705A>T
CA402990203
NM_000156.6:c.705A>C