Canonical Allele Identifier: PA645402016
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2369Ser
CA046951
NM_001127510.3:c.7105C>T