Canonical Allele Identifier: PA2579797052
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ala237Ser
CA410600523
NM_000071.3:c.709G>T
CA2579812976
NM_000071.3:c.709_710delinsAG
CA2579812977
NM_000071.3:c.709_711delinsTCC
CA2579813904
NM_000071.3:c.709_711delinsTCA