Canonical Allele Identifier: PA2825630222
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1108Lys
CA16028623
NM_001127510.3:c.3324T>A
CA16028624
NM_001127510.3:c.3324T>G