Canonical Allele Identifier: PA2827986819
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1051201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1609Ser
CA040262
NM_001354900.2:c.4826A>G