Canonical Allele Identifier: PA2828019615
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Asn1007Lys
CA16028623
NM_001354903.2:c.3021T>A
CA16028624
NM_001354903.2:c.3021T>G