Canonical Allele Identifier: PA2827955289
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His317Gln
CA16023326
NM_001354897.2:c.951T>A
CA16023327
NM_001354897.2:c.951T>G