Canonical Allele Identifier: PA2827962190
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2561155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2502Phe
CA16037595
NM_001354897.2:c.7505C>T