Canonical Allele Identifier: PA2828035518
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Pro739Ser
CA007632
NM_001354904.2:c.2215C>T