Canonical Allele Identifier: PA2827962816
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2690Ala
CA014255
NM_001354897.2:c.8068C>G