Canonical Allele Identifier: PA2828019642
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Val842Ala
CA008333
NM_001354906.2:c.2525T>C