Canonical Allele Identifier: PA2828023583
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1717624
ClinVar RCV Id: RCV003743868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ala1624Ser
CA16032639
NM_001354903.2:c.4870G>T