Canonical Allele Identifier: PA2579796533
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Asn212Thr
CA410600850
NM_000071.3:c.635A>C
CA2579812277
NM_000071.3:c.635_636delinsCT
CA2579812278
NM_000071.3:c.635_636delinsCG