Canonical Allele Identifier: PA2827961900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2413Pro
CA10578440
NM_001354897.2:c.7238A>C