Canonical Allele Identifier: PA2828011375
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2192Asn
CA16036703
NM_001354905.2:c.6575G>A