Canonical Allele Identifier: PA2827973414
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470154
ClinVar RCV Id: RCV001019030 RCV003999446 RCV003537095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.His279Gln
CA16023326
NM_001354899.2:c.837T>A
CA16023327
NM_001354899.2:c.837T>G