Canonical Allele Identifier: PA2827967890
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135702

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr1420Ala
CA009444
NM_001354898.2:c.4258A>G