Canonical Allele Identifier: PA2826247348
Gene: ST20-MTHFS HGNC NCBI

Linked Data

ClinVar Variation Id: 2038284
ClinVar RCV Id: RCV002890631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186689.1:p.Thr178Ala
CA7690251
NM_001199760.2:c.532A>G