Canonical Allele Identifier: PA645398977
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Tyr737His
CA031174
NM_001127510.3:c.2209T>C