ClinGen Allele Registry
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Canonical Allele Identifier:
PA916024472
Gene: CBS
HGNC
NCBI
Linked Data
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Transcript change
NP_001307227.1:p.Ser466Leu
NM_001320298.2:c.1396_1397delinsCT
NM_001320298.2:c.1397C>T
NM_001320298.2:c.1397_1398delinsTA