Canonical Allele Identifier: PA2827957261
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233468

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1015Val
CA10578347
NM_001354897.2:c.3044C>T