Canonical Allele Identifier: PA2828002681
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala1579Val
CA009818
NM_001354902.2:c.4736C>T