Canonical Allele Identifier: PA297803
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181799
ClinVar RCV Id: RCV000159547 RCV000211907 RCV000234536 RCV003315947 RCV002307414
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1064Ser
CA008176
NM_001127511.3:c.3191C>G
CA16028451
NM_001127511.3:c.3190A>T