Canonical Allele Identifier: PA2579799970
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ala38Asp
CA410602420
NM_000071.3:c.113C>A
CA2579812809
NM_000071.3:c.113_114delinsAT