Canonical Allele Identifier: PA2827971956
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2655Ser
CA16038785
NM_001354898.2:c.7963C>T