Canonical Allele Identifier: PA2573300053
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1448647
ClinVar RCV Id: RCV002002298

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_620279.1:p.Pro40Ser
CA304067305
NM_138924.3:c.118C>T