Canonical Allele Identifier: PA2827962601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760901
ClinVar RCV Id: RCV002412214

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2628Thr
CA16038395
NM_001354897.2:c.7883A>C