Canonical Allele Identifier: PA2827980469
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro2454Ala
CA013688
NM_001354899.2:c.7360C>G