Canonical Allele Identifier: PA1139741869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 953942
ClinVar RCV Id: RCV003650782

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Lys2601Asn
CA16038162
NM_001354896.2:c.7803A>C
CA16038163
NM_001354896.2:c.7803A>T