Canonical Allele Identifier: PA1139678002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 843820

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn999Asp
CA16028009
NM_001127511.3:c.2995A>G