Canonical Allele Identifier: PA2828011500
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231537
ClinVar RCV Id: RCV003534521 RCV000218412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Gln2216His
CA047019
NM_001354905.2:c.6648G>C
CA16036857
NM_001354905.2:c.6648G>T