Canonical Allele Identifier: PA338666
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216181
ClinVar RCV Id: RCV000775352 RCV003765284 RCV003996980
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn2618Asp
CA338662
NM_000038.6:c.7852A>G