Canonical Allele Identifier: PA916041576
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 654022
ClinVar RCV Id: RCV003653372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu2621Asp
CA16038295
NM_001354896.2:c.7863A>C
CA16038296
NM_001354896.2:c.7863A>T