Canonical Allele Identifier: PA2828049021
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1003325
ClinVar RCV Id: RCV003538647

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser2526Ala
CA16038604
NM_001354904.2:c.7576T>G