Canonical Allele Identifier: PA2827963157
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2795His
CA050563
NM_001354897.2:c.8383A>C