Canonical Allele Identifier: PA2828019082
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1721460
ClinVar RCV Id: RCV003743922
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Lys929Asn
CA16028099
NM_001354903.2:c.2787A>C
CA16028100
NM_001354903.2:c.2787A>T