Canonical Allele Identifier: PA2828001547
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1021385
ClinVar RCV Id: RCV003770736 RCV004035024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn1017Lys
CA16028623
NM_001354902.2:c.3051T>A
CA16028624
NM_001354902.2:c.3051T>G