Canonical Allele Identifier: PA2827965321
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn635Ser
CA16025642
NM_001354898.2:c.1904A>G