Canonical Allele Identifier: PA2828054795
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro705Ser
CA007632
NM_001354905.2:c.2113C>T