Canonical Allele Identifier: PA2825636458
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714967
ClinVar RCV Id: RCV003743845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr628Ser
CA16025436
NM_001127510.3:c.1882A>T
CA16025438
NM_001127510.3:c.1883C>G