Canonical Allele Identifier: PA916041903
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181785

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Arg424His
CA004108
NM_001354897.2:c.1271G>A