Canonical Allele Identifier: PA2825580989
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 2883542
ClinVar RCV Id: RCV003757997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108454.1:p.Ser271Leu
CA89746785
NM_001114982.2:c.812C>T