Canonical Allele Identifier: PA2827944691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro1634Leu
CA040139
NM_001354895.2:c.4901C>T