Canonical Allele Identifier: PA2825020412
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Pro1467Ser
CA038968
NM_000038.6:c.4399C>T