Canonical Allele Identifier: PA2579793582
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ala8Ser
CA410602601
NM_000071.3:c.22G>T
CA2579812233
NM_000071.3:c.22_24delinsAGT
CA2579812235
NM_000071.3:c.22_24delinsTCG