Canonical Allele Identifier: PA658660837
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2622Arg
CA16038423
NM_001127510.3:c.7865C>G