Canonical Allele Identifier: PA2580281037
Gene: PNN HGNC NCBI

Linked Data

ClinVar Variation Id: 2327049
ClinVar RCV Id: RCV004171698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002678.3:p.Lys699Thr
CA389550086
NM_002687.4:c.2096A>C