Canonical Allele Identifier: PA2828011784
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_001341831.1:p.Lys2321Asn
CA16037092
NM_001354902.2:c.6963A>C
CA16037093
NM_001354902.2:c.6963A>T