Canonical Allele Identifier: PA891859962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570044

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile990Val
CA16027942
NM_001127511.3:c.2968A>G