Canonical Allele Identifier: PA891859204
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Gly972Ser
CA033918
NM_001127510.3:c.2914G>A