Canonical Allele Identifier: PA916041600
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Pro2640Ala
CA16038420
NM_001354896.2:c.7918C>G