Canonical Allele Identifier: PA2828019605
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1006Ser
CA16028614
NM_001354903.2:c.3016G>T