Canonical Allele Identifier: PA916041952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.His454Arg
CA004248
NM_001354897.2:c.1361A>G