Canonical Allele Identifier: PA2825644613
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 927906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys2572Asn
CA16038210
NM_001127511.3:c.7716A>C
CA16038211
NM_001127511.3:c.7716A>T