Canonical Allele Identifier: PA2827947091
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2369Leu
CA16036808
NM_001354895.2:c.7106C>T