Canonical Allele Identifier: PA2827989145
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2587029
ClinVar RCV Id: RCV003339110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2320Pro
CA16036756
NM_001354900.2:c.6958T>C