Canonical Allele Identifier: PA151443
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127295
ClinVar Variation Id: 3001945
ClinVar RCV Id: RCV003863008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys1436Glu
CA009483
NM_001127511.3:c.4306A>G
CA2740094004
NM_001127511.3:c.4305_4306delinsCG