Canonical Allele Identifier: PA2579801021
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Pro422Ser
CA410397329
NM_000071.3:c.1264C>T
CA2579805176
NM_000071.3:c.1264_1266delinsTCA
CA2579805178
NM_000071.3:c.1264_1266delinsTCT
CA2579813502
NM_000071.3:c.1264_1266delinsAGT