Canonical Allele Identifier: PA2825639455
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Leu904Phe
CA033363
NM_001127511.3:c.2710C>T