Canonical Allele Identifier: PA2579801433
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys441Thr
CA410397024
NM_000071.3:c.1322A>C
CA2579806758
NM_000071.3:c.1322_1323delinsCT