Canonical Allele Identifier: PA16039911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala1005Val
CA10578347
NM_000038.6:c.3014C>T