Canonical Allele Identifier: PA2579801322
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Glu436Asp
CA410397082
NM_000071.3:c.1308G>T
CA410397084
NM_000071.3:c.1308G>C