Canonical Allele Identifier: PA2579795767
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Glu176Arg
CA2579810160
NM_000071.3:c.526_527delinsAG
CA2579810161
NM_000071.3:c.526_527delinsCG
CA2579810162
NM_000071.3:c.526_528delinsCGT