Canonical Allele Identifier: PA2825633367
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949271
ClinVar RCV Id: RCV003650743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1650Tyr
CA16032166
NM_001127510.3:c.4948A>T