Canonical Allele Identifier: PA658660551
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn2405His
CA16037039
NM_001127510.3:c.7213A>C