Canonical Allele Identifier: PA2827941400
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714967
ClinVar RCV Id: RCV003743845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Thr628Ser
CA16025436
NM_001354895.2:c.1882A>T
CA16025438
NM_001354895.2:c.1883C>G