Canonical Allele Identifier: PA2827990167
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761618
ClinVar RCV Id: RCV002419191

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2628Ala
CA16038722
NM_001354900.2:c.7882C>G