Canonical Allele Identifier: PA2499252118
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1668Ser
CA040262
NM_001354896.2:c.5003A>G