Canonical Allele Identifier: PA156882
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133537
ClinVar RCV Id: RCV000120047 RCV000163521 RCV000199434 RCV000677785 RCV000677786 RCV000677787 RCV001704030 RCV003952585
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2778Ser
CA014561
NM_000038.6:c.8332G>T