Canonical Allele Identifier: PA2827968537
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Arg1615Trp
CA009806
NM_001354898.2:c.4843C>T