Canonical Allele Identifier: PA2579798414
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr300Asn
CA410600047
NM_000071.3:c.899C>A
CA2579804073
NM_000071.3:c.899_900delinsAT