Canonical Allele Identifier: PA2579796980
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Tyr233Asn
CA410600571
NM_000071.3:c.697T>A
CA2579803516
NM_000071.3:c.697_699delinsAAT