Canonical Allele Identifier: PA2826131973
Gene: BHMT2 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171476.1:p.Arg201Ile
CA360218901
NM_001178005.2:c.602G>T