Canonical Allele Identifier: PA2827962206
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2507Trp
CA16037624
NM_001354897.2:c.7520C>G