Canonical Allele Identifier: PA2828003971
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482426

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn2314His
CA16037039
NM_001354902.2:c.6940A>C