Canonical Allele Identifier: PA2827264779
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1062831
ClinVar RCV Id: RCV001372592
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Arg171Ser
CA355755203
NM_001329146.2:c.513A>C
CA355755204
NM_001329146.2:c.513A>T