Canonical Allele Identifier: PA2825636299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2013889
ClinVar RCV Id: RCV003742943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser546Cys
CA16024882
NM_001127510.3:c.1636A>T
CA2580072447
NM_001127510.3:c.1635_1636delinsAT