Canonical Allele Identifier: PA891859840
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2665Ser
CA16038695
NM_001127510.3:c.7993C>T