Canonical Allele Identifier: PA916041367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482462
ClinVar RCV Id: RCV000572004
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys2430Asn
CA16037092
NM_001354896.2:c.7290A>C
CA16037093
NM_001354896.2:c.7290A>T