Canonical Allele Identifier: PA2827971735
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2593Ser
CA16038396
NM_001354898.2:c.7778A>G