Canonical Allele Identifier: PA2827962545
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2609Asn
CA014071
NM_001354897.2:c.7827A>C
CA16038265
NM_001354897.2:c.7827A>T