Canonical Allele Identifier: PA2579798299
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln295Leu
CA410600079
NM_000071.3:c.884A>T
CA2579810764
NM_000071.3:c.884_885delinsTT
CA2579810765
NM_000071.3:c.883_884delinsTT
CA2579810766
NM_000071.3:c.883_885delinsTTA