Canonical Allele Identifier: PA215499
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala717Val
CA007259
NM_001127511.3:c.2150C>T