Canonical Allele Identifier: PA2825018916
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Tyr1135Cys
CA035239
NM_000038.6:c.3404A>G