Canonical Allele Identifier: PA2825024857
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2601Asn
CA16038277
NM_000038.6:c.7802G>A