Canonical Allele Identifier: PA2827955712
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr506Ile
CA16024566
NM_001354897.2:c.1517C>T