Canonical Allele Identifier: PA2827959992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val1832Gly
CA10578404
NM_001354897.2:c.5495T>G