Canonical Allele Identifier: PA2827947336
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 971797
ClinVar RCV Id: RCV003652111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Phe2443Leu
CA16037285
NM_001354895.2:c.7327T>C
CA16037290
NM_001354895.2:c.7329C>A
CA16037291
NM_001354895.2:c.7329C>G