Canonical Allele Identifier: PA2827966867
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181801
ClinVar RCV Id: RCV000159549 RCV000211910 RCV000586988 RCV001818351 RCV003534406 RCV003998412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Lys1114Gln
CA008372
NM_001354898.2:c.3340A>C