Canonical Allele Identifier: PA2579801071
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr424Ile
CA410397291
NM_000071.3:c.1271C>T
CA2579803839
NM_000071.3:c.1271_1272delinsTA
CA2579803840
NM_000071.3:c.1271_1272delinsTT