Canonical Allele Identifier: PA2827980405
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569210

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2436Cys
CA16037430
NM_001354899.2:c.7307C>G