Canonical Allele Identifier: PA2579795616
Gene: CBS HGNC NCBI

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000062.1:p.Met169Val
CA410601364
NM_000071.3:c.505A>G
CA2579813543
NM_000071.3:c.505_507delinsGTT