Canonical Allele Identifier: PA2827977496
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2080747

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Glu1545Asp
CA16031680
NM_001354899.2:c.4635A>C
CA16031681
NM_001354899.2:c.4635A>T