Canonical Allele Identifier: PA916041275
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418637

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn2358His
CA046653
NM_001354896.2:c.7072A>C