Canonical Allele Identifier: PA2826131956
Gene: BHMT2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171476.1:p.Gly42Arg
CA360212517
NM_001178005.2:c.124G>A
CA360212520
NM_001178005.2:c.124G>C