Canonical Allele Identifier: PA2579798309
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Gln295His
CA410600077
NM_000071.3:c.885G>T
CA410600078
NM_000071.3:c.885G>C