Canonical Allele Identifier: PA2825641711
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1632Ser
CA040262
NM_001127511.3:c.4895A>G