Canonical Allele Identifier: PA156856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133532

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly1685Ala
CA009873
NM_001127511.3:c.5054G>C