Canonical Allele Identifier: PA2579792016
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asp494Tyr
CA410395863
NM_000071.3:c.1480G>T
CA2579811188
NM_000071.3:c.1480_1482delinsTAT