Canonical Allele Identifier: PA2825644317
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2561155

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2474Phe
CA16037595
NM_001127511.3:c.7421C>T