Canonical Allele Identifier: PA2827969436
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 219739
ClinVar RCV Id: RCV000204791 RCV000481360 RCV000574367 RCV003316131 RCV003417741 RCV003997579
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile1893Val
CA042868
NM_001354898.2:c.5677A>G