Canonical Allele Identifier: PA891859770
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 575302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu2507Phe
CA16037679
NM_001127510.3:c.7519C>T