Canonical Allele Identifier: PA2828013092
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro2462Ala
CA16038420
NM_001354905.2:c.7384C>G