Canonical Allele Identifier: PA2827986873
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1629Val
CA009818
NM_001354900.2:c.4886C>T