Canonical Allele Identifier: PA645402339
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro2622Ala
CA16038420
NM_001127510.3:c.7864C>G