Canonical Allele Identifier: PA2828027584
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Leu2241Phe
CA046700
NM_001354903.2:c.6723A>C
CA16036647
NM_001354903.2:c.6723A>T