Canonical Allele Identifier: PA16040104
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232940

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro2369Ser
CA046951
NM_000038.6:c.7105C>T