Canonical Allele Identifier: PA2827973828
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val414Asp
CA16024206
NM_001354899.2:c.1241T>A