Canonical Allele Identifier: PA2827971349
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2472Trp
CA16037624
NM_001354898.2:c.7415C>G