Canonical Allele Identifier: PA2579794786
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro2Thr
CA410602638
NM_000071.3:c.4C>A
CA2579805282
NM_000071.3:c.4_6delinsACG