Canonical Allele Identifier: PA1139736369
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 919879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn620Ser
CA16025270
NM_001354896.2:c.1859A>G