Canonical Allele Identifier: PA1139741759
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 935616
ClinVar RCV Id: RCV003650667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.His2544Tyr
CA16037795
NM_001354896.2:c.7630C>T