Canonical Allele Identifier: PA2579796719
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asp221Ser
CA2579811989
NM_000071.3:c.661_663delinsAGT
CA2579811990
NM_000071.3:c.661_663delinsTCG
CA2579811991
NM_000071.3:c.661_662delinsTC
CA2579811992
NM_000071.3:c.661_663delinsTCT