Canonical Allele Identifier: PA2825638385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2748653
ClinVar RCV Id: RCV003536633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser528Gly
CA16024881
NM_001127511.3:c.1582A>G
CA2697546184
NM_001127511.3:c.1581_1582delinsAG