Canonical Allele Identifier: PA2827977107
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Pro1430Ser
CA009490
NM_001354899.2:c.4288C>T