Canonical Allele Identifier: PA2828007158
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1490Ser
CA040262
NM_001354905.2:c.4469A>G