Canonical Allele Identifier: PA2579795495
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His17Ser
CA2579808851
NM_000071.3:c.49_51delinsTCT
CA2579808852
NM_000071.3:c.49_51delinsTCG
CA2579808853
NM_000071.3:c.49_50delinsTC
CA2579808855
NM_000071.3:c.49_51delinsAGT