Canonical Allele Identifier: PA916041307
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2387Leu
CA16036808
NM_001354896.2:c.7160C>T