Canonical Allele Identifier: PA16040087
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn2220Asp
CA045646
NM_000038.6:c.6658A>G