Canonical Allele Identifier: PA916041448
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2500Ala
CA013688
NM_001354896.2:c.7498C>G