Canonical Allele Identifier: PA658660203
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482374

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asp1871Tyr
CA042401
NM_001127510.3:c.5611G>T