Canonical Allele Identifier: PA2827962256
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Leu2521Phe
CA013771
NM_001354897.2:c.7561C>T