Canonical Allele Identifier: PA658687624
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1667Asp
CA040350
NM_001127510.3:c.4999A>G