Canonical Allele Identifier: PA2827994261
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41503
ClinVar RCV Id: RCV000034385 RCV000130655 RCV000148371 RCV000204291 RCV000235094 RCV003407396 RCV003996153 RCV003534315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Thr1101Lys
CA008452
NM_001354901.2:c.3302C>A