Canonical Allele Identifier: PA2828029689
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro2564Ser
CA16038695
NM_001354903.2:c.7690C>T