Canonical Allele Identifier: PA2827986358
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1471Asn
CA009616
NM_001354900.2:c.4411G>A