Canonical Allele Identifier: PA2825634822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1336346

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2346Leu
CA16036672
NM_001127510.3:c.7037C>T