Canonical Allele Identifier: PA2579792158
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His501Ala
CA2579809161
NM_000071.3:c.1501_1503delinsGCG
CA2579809163
NM_000071.3:c.1501_1503delinsGCT