Canonical Allele Identifier: PA272852
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg1622Trp
CA009806
NM_001127511.3:c.4864C>T