Canonical Allele Identifier: PA2827990862
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Leu34His
CA10578288
NM_001354901.2:c.101T>A