Canonical Allele Identifier: PA2579792135
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ser500Ala
CA410395774
NM_000071.3:c.1498T>G
CA2579805312
NM_000071.3:c.1498_1500delinsGCT