Canonical Allele Identifier: PA2579794274
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gly11Arg
CA410602584
NM_000071.3:c.31G>A
CA410602585
NM_000071.3:c.31G>C
CA2579810099
NM_000071.3:c.31_33delinsCGT
CA2579810100
NM_000071.3:c.31_33delinsCGA
CA2579810101
NM_000071.3:c.31_33delinsAGA