Canonical Allele Identifier: PA2827976054
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1114Thr
CA035313
NM_001354899.2:c.3341A>C