Canonical Allele Identifier: PA2827975983
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1096Ser
CA16028720
NM_001354899.2:c.3287A>G