Canonical Allele Identifier: PA2825580191
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600884
ClinVar RCV Id: RCV002124758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Met122Ile
CA2752217
NM_001114980.1:c.366G>C
CA2752218
NM_001114980.1:c.366G>A
CA355753349
NM_001114980.1:c.366G>T