Canonical Allele Identifier: PA2825025632
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2799Pro
CA16039553
NM_000038.6:c.8395T>C