Canonical Allele Identifier: PA2579796400
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro21Thr
CA410602528
NM_000071.3:c.61C>A
CA2579806584
NM_000071.3:c.61_63delinsACT