Canonical Allele Identifier: PA2828010952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 644645

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser2135Ala
CA16036352
NM_001354905.2:c.6403T>G