Canonical Allele Identifier: PA2828047942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Leu2385Phe
CA013771
NM_001354904.2:c.7153C>T