Canonical Allele Identifier: PA658660505
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470078
ClinVar RCV Id: RCV000568097 RCV002527860 RCV002483459 RCV003222032 RCV003999423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2379Ser
CA047031
NM_001127510.3:c.7136C>G
CA16036872
NM_001127510.3:c.7135A>T