Canonical Allele Identifier: PA2579792157
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.His501Ser
CA2579809139
NM_000071.3:c.1501_1503delinsTCG
CA2579809141
NM_000071.3:c.1501_1503delinsTCT
CA2579809142
NM_000071.3:c.1501_1503delinsAGT