Canonical Allele Identifier: PA2827997567
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro2111Ser
CA16035571
NM_001354901.2:c.6331C>T