Canonical Allele Identifier: PA2827961925
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482462
ClinVar RCV Id: RCV000572004

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2422Asn
CA16037092
NM_001354897.2:c.7266A>C
CA16037093
NM_001354897.2:c.7266A>T