Canonical Allele Identifier: PA658689322
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2601Asn
CA16038277
NM_001127510.3:c.7802G>A