Canonical Allele Identifier: PA174636
Gene: CDKN2AIP HGNC NCBI

Linked Data

ClinVar Variation Id: 161707
ClinVar RCV Id: RCV000149243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060102.1:p.Leu305Arg
CA174635
NM_017632.4:c.914T>G