Canonical Allele Identifier: PA163615
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala1670Val
CA009818
NM_001127510.3:c.5009C>T