Canonical Allele Identifier: PA2579795645
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro170Leu
CA410601342
NM_000071.3:c.509C>T
CA2579805878
NM_000071.3:c.509_510delinsTT
CA2579805880
NM_000071.3:c.509_510delinsTG