Canonical Allele Identifier: PA2826131961
Gene: BHMT2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171476.1:p.Phe63Leu
CA360213064
NM_001178005.2:c.187T>C
CA360213074
NM_001178005.2:c.189C>A
CA360213077
NM_001178005.2:c.189C>G