Canonical Allele Identifier: PA2827989165
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2328Leu
CA16036808
NM_001354900.2:c.6983C>T