Canonical Allele Identifier: PA2827980191
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188173
ClinVar RCV Id: RCV000168076 RCV000486411 RCV000491288 RCV000657134 RCV003316065 RCV003995605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2370Phe
CA012909
NM_001354899.2:c.7109C>T