Canonical Allele Identifier: PA2828004168
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220176
ClinVar RCV Id: RCV000203815 RCV000561106 RCV000587117 RCV001002346 RCV003316138 RCV003997620
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.His2441Tyr
CA048637
NM_001354902.2:c.7321C>T