Canonical Allele Identifier: PA2827980856
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys2571Asn
CA014071
NM_001354899.2:c.7713A>C
CA16038265
NM_001354899.2:c.7713A>T