Canonical Allele Identifier: PA2827264456
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1413071
ClinVar RCV Id: RCV001925684
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316074.1:p.Thr97Ser
CA355750847
NM_001329145.2:c.289A>T
CA355750849
NM_001329145.2:c.290C>G