Canonical Allele Identifier: PA2579801079
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr424Pro
CA410397300
NM_000071.3:c.1270A>C
CA2579803832
NM_000071.3:c.1270_1272delinsCCT
CA2579803835
NM_000071.3:c.1270_1272delinsCCG