Canonical Allele Identifier: PA191264
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185188
ClinVar RCV Id: RCV000164557 RCV001697165 RCV003743612 RCV003995350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala61Thr
CA006037
NM_001127510.3:c.181G>A