Canonical Allele Identifier: PA2827971161
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 971797
ClinVar RCV Id: RCV003652111
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Phe2418Leu
CA16037285
NM_001354898.2:c.7252T>C
CA16037290
NM_001354898.2:c.7254C>A
CA16037291
NM_001354898.2:c.7254C>G