Canonical Allele Identifier: PA096561
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 188989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Lys102Asn
CA274220
NM_000071.3:c.306G>C
CA410602002
NM_000071.3:c.306G>T