Canonical Allele Identifier: PA916041574
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629231
ClinVar RCV Id: RCV000773930

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln2618His
CA16038272
NM_001354896.2:c.7854A>C
CA16038273
NM_001354896.2:c.7854A>T