Canonical Allele Identifier: PA16040128
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231400

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn2510Ser
CA10578446
NM_000038.6:c.7529A>G