Canonical Allele Identifier: PA2827990607
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236656
ClinVar RCV Id: RCV001017724 RCV003535648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln2763His
CA10582345
NM_001354900.2:c.8289G>T
CA16039584
NM_001354900.2:c.8289G>C