Canonical Allele Identifier: PA2579796429
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Ala207Gly
CA410600894
NM_000071.3:c.620C>G
CA2579813069
NM_000071.3:c.620_621delinsGT
CA2579813070
NM_000071.3:c.620_621delinsGG