Canonical Allele Identifier: PA2827972068
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82636
ClinVar RCV Id: RCV000073625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met2688Leu
CA014373
NM_001354898.2:c.8062A>C
CA16039003
NM_001354898.2:c.8062A>T