Canonical Allele Identifier: PA16039900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu93His
CA10578288
NM_000038.6:c.278T>A