Canonical Allele Identifier: PA2828009521
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1010431
ClinVar RCV Id: RCV002241885 RCV002341616
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Val1617Leu
CA16032525
NM_001354902.2:c.4849G>C
CA16032526
NM_001354902.2:c.4849G>T