Canonical Allele Identifier: PA2827947909
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asn2618Ser
CA16038396
NM_001354895.2:c.7853A>G