Canonical Allele Identifier: PA2827970659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41534
ClinVar RCV Id: RCV000034419 RCV000131637 RCV000168325 RCV000211931 RCV001151804 RCV001353490 RCV003743553 RCV003996165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gln2266His
CA012603
NM_001354898.2:c.6798A>T
CA16036332
NM_001354898.2:c.6798A>C