Canonical Allele Identifier: PA2827946423
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Pro2170Ser
CA16035571
NM_001354895.2:c.6508C>T