Canonical Allele Identifier: PA2827961813
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470078
ClinVar RCV Id: RCV000568097 RCV002527860 RCV002483459 RCV003222032 RCV003999423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr2389Ser
CA047031
NM_001354897.2:c.7166C>G
CA16036872
NM_001354897.2:c.7165A>T