Canonical Allele Identifier: PA2828003967
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gln2312Pro
CA10578440
NM_001354902.2:c.6935A>C