Canonical Allele Identifier: PA2579794674
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Thr13Ala
CA410602574
NM_000071.3:c.37A>G
CA2579804363
NM_000071.3:c.37_39delinsGCG
CA2579804364
NM_000071.3:c.37_39delinsGCT