Canonical Allele Identifier: PA215526
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1458Ser
CA009490
NM_001127510.3:c.4372C>T