Canonical Allele Identifier: PA2825643305
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2152Ser
CA16035571
NM_001127511.3:c.6454C>T