Canonical Allele Identifier: PA2825643932
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2351Leu
CA16036808
NM_001127511.3:c.7052C>T