Canonical Allele Identifier: PA2828007934
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 631456
ClinVar RCV Id: RCV000777890
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Val1616Leu
CA16032974
NM_001354905.2:c.4846G>C
CA16032975
NM_001354905.2:c.4846G>T