Canonical Allele Identifier: PA2827996029
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1745286
ClinVar RCV Id: RCV002335948 RCV003476960 RCV003743971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asp1639Val
CA16032466
NM_001354901.2:c.4916A>T