Canonical Allele Identifier: PA2827964719
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Leu431Phe
CA10578315
NM_001354898.2:c.1291C>T