Canonical Allele Identifier: PA2827947760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760274
ClinVar RCV Id: RCV002400650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser2571Tyr
CA16038083
NM_001354895.2:c.7712C>A