Canonical Allele Identifier: PA2579800783
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His411Ser
CA2579808725
NM_000071.3:c.1231_1233delinsTCT
CA2579808726
NM_000071.3:c.1231_1233delinsAGT
CA2579808727
NM_000071.3:c.1231_1233delinsTCG