Canonical Allele Identifier: PA2825024918
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 652208

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn2618Ser
CA16038396
NM_000038.6:c.7853A>G