Canonical Allele Identifier: PA2828008848
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41530

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro1367Ser
CA009490
NM_001354902.2:c.4099C>T