Canonical Allele Identifier: PA645402358
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 350423
ClinVar RCV Id: RCV000261598 RCV000478957 RCV000575871 RCV003995887 RCV003766024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2635Ala
CA10622269
NM_001127510.3:c.7903A>G