Canonical Allele Identifier: PA2579795264
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ile152Val
CA410601534
NM_000071.3:c.454A>G
CA2579808541
NM_000071.3:c.454_456delinsGTG
CA2579808543
NM_000071.3:c.454_456delinsGTT