Canonical Allele Identifier: PA645510058
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Tyr1027Asp
CA16028076
NM_001127510.3:c.3079T>G