Canonical Allele Identifier: PA314869
Gene: GATM HGNC NCBI

Linked Data

ClinVar Variation Id: 205613
ClinVar RCV Id: RCV000437121 RCV001082642 RCV001251999 RCV002317103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001473.1:p.Thr136Met
CA314868
NM_001482.3:c.407C>T