Canonical Allele Identifier: PA2828013394
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1025683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2509Ser
CA16038723
NM_001354905.2:c.7525C>T