Canonical Allele Identifier: PA2825016451
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Tyr737His
CA031174
NM_000038.6:c.2209T>C