Canonical Allele Identifier: PA2828005373
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro350Thr
CA16024197
NM_001354902.2:c.1048C>A