Canonical Allele Identifier: PA2827979829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41534
ClinVar RCV Id: RCV000034419 RCV000131637 RCV000168325 RCV000211931 RCV001151804 RCV001353490 RCV003743553 RCV003996165
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Gln2263His
CA012603
NM_001354899.2:c.6789A>T
CA16036332
NM_001354899.2:c.6789A>C