Canonical Allele Identifier: PA2828008194
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn1669Ser
CA042093
NM_001354905.2:c.5006A>G