Canonical Allele Identifier: PA2579796987
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Tyr233His
CA410600572
NM_000071.3:c.697T>C
CA2579803512
NM_000071.3:c.697_699delinsCAT