Canonical Allele Identifier: PA2825637649
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822781
ClinVar RCV Id: RCV001018420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser277Arg
CA16023248
NM_001127511.3:c.829A>C
CA16023252
NM_001127511.3:c.831T>A
CA16023253
NM_001127511.3:c.831T>G