Canonical Allele Identifier: PA2828017049
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2125861
ClinVar RCV Id: RCV003744997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys453Asn
CA16026168
NM_001354906.2:c.1359G>C
CA16026169
NM_001354906.2:c.1359G>T