Canonical Allele Identifier: PA2825641144
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro1449Ser
CA038968
NM_001127511.3:c.4345C>T