Canonical Allele Identifier: PA2828007947
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 576430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1619Val
CA16032994
NM_001354905.2:c.4855A>G