Canonical Allele Identifier: PA916042210
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His260Arg
CA16022971
NM_001354902.2:c.779A>G