Canonical Allele Identifier: PA1139741523
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 852832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2395His
CA16036858
NM_001354896.2:c.7183A>C