Canonical Allele Identifier: PA2827961777
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2379Ser
CA046951
NM_001354897.2:c.7135C>T