Canonical Allele Identifier: PA2827998677
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759217
ClinVar RCV Id: RCV002391623 RCV003534881
ClinVar Variation Id: 1759218
ClinVar RCV Id: RCV002391624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Gln2441His
CA16037641
NM_001354901.2:c.7323G>C
CA16037642
NM_001354901.2:c.7323G>T