Canonical Allele Identifier: PA2826247348
Gene: ST20-MTHFS HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

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