Canonical Allele Identifier: PA2827978167
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1750Arg
CA16032991
NM_001354899.2:c.5249C>G