Canonical Allele Identifier: PA2827980042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2324Asn
CA16036703
NM_001354899.2:c.6971G>A