Canonical Allele Identifier: PA2827958752
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186279

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1455Ile
CA009453
NM_001354897.2:c.4364C>T