Canonical Allele Identifier: PA2827977140
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1439Ser
CA038968
NM_001354899.2:c.4315C>T