Canonical Allele Identifier: PA916071385
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 664322
ClinVar RCV Id: RCV000822400 RCV001830817
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Asn170Thr
CA9043623
NM_138924.3:c.509A>C