Canonical Allele Identifier: PA658660744
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487041

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2540Ala
CA16037879
NM_001127510.3:c.7618C>G