Canonical Allele Identifier: PA323233
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 212855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ile286Val
CA323231
NM_000071.3:c.856A>G
CA2579808216
NM_000071.3:c.856_858delinsGTA
CA2579808217
NM_000071.3:c.856_858delinsGTT