Canonical Allele Identifier: PA2828042537
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629228
ClinVar RCV Id: RCV000773927
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Gly1595Val
CA16032616
NM_001354904.2:c.4784G>T