Canonical Allele Identifier: PA190792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185017
ClinVar RCV Id: RCV000164369 RCV000236978 RCV000545398 RCV000679080 RCV003534440 RCV003995337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.His2149Pro
CA011185
NM_001127510.3:c.6446A>C