Canonical Allele Identifier: PA2827973726
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg386His
CA004108
NM_001354899.2:c.1157G>A