Canonical Allele Identifier: PA2579801137
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Trp43Cys
CA410602384
NM_000071.3:c.129G>T
CA410602385
NM_000071.3:c.129G>C