Canonical Allele Identifier: PA348299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220569
ClinVar RCV Id: RCV000204027 RCV001018168 RCV003997646
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser992Asn
CA348296
NM_001127511.3:c.2975G>A