Canonical Allele Identifier: PA211362
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41503

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr1142Lys
CA008452
NM_001127511.3:c.3425C>A