Canonical Allele Identifier: PA2827976041
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1731224
ClinVar RCV Id: RCV002452204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys1111Asn
CA16028823
NM_001354899.2:c.3333G>C
CA16028824
NM_001354899.2:c.3333G>T