Canonical Allele Identifier: PA2579798378
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr299Ser
CA410600054
NM_000071.3:c.895A>T
CA2579804084
NM_000071.3:c.895_897delinsTCG
CA2579804085
NM_000071.3:c.896_897delinsGT
CA2579804087
NM_000071.3:c.895_897delinsTCT