Canonical Allele Identifier: PA2828042498
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn1590Ser
CA040767
NM_001354904.2:c.4769A>G