Canonical Allele Identifier: PA2827941399
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 572572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn627Ser
CA16025430
NM_001354895.2:c.1880A>G