Canonical Allele Identifier: PA916024461
Gene: CBS HGNC NCBI

Linked Data

ClinVar Variation Id: 551308
ClinVar RCV Id: RCV000666335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307227.1:p.Ile435Thr
CA410397108
NM_001320298.2:c.1304T>C
CA2579808102
NM_001320298.2:c.1304_1305delinsCA