Canonical Allele Identifier: PA2827970942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 852832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2352His
CA16036858
NM_001354898.2:c.7054A>C