Canonical Allele Identifier: PA2827986775
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 183069
ClinVar RCV Id: RCV000161934 RCV000236412 RCV000568367 RCV003998534 RCV003315967 RCV003398826
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp1595Tyr
CA009798
NM_001354900.2:c.4783G>T