Canonical Allele Identifier: PA2827998909
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile2514Val
CA013990
NM_001354901.2:c.7540A>G