Canonical Allele Identifier: PA2827959483
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1680Val
CA009818
NM_001354897.2:c.5039C>T