Canonical Allele Identifier: PA2579798125
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Leu287Phe
CA410600131
NM_000071.3:c.859C>T
CA645601864
NM_000071.3:c.858_859delinsTT
CA2579807604
NM_000071.3:c.859_861delinsTTT