Canonical Allele Identifier: PA156808
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522
ClinVar RCV Id: RCV000120032 RCV000131590 RCV000587624 RCV001153055 RCV003323291
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2497Leu
CA013717
NM_001127510.3:c.7490C>T