Canonical Allele Identifier: PA2827971593
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile2548Val
CA013990
NM_001354898.2:c.7642A>G