Canonical Allele Identifier: PA2827991822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3231519
ClinVar RCV Id: RCV004525590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His329Gln
CA16023852
NM_001354901.2:c.987C>A
CA16023853
NM_001354901.2:c.987C>G