Canonical Allele Identifier: PA2827939738
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser102Pro
CA034347
NM_001354895.2:c.304T>C