Canonical Allele Identifier: PA2825579627
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1600884
ClinVar RCV Id: RCV002124758

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Met216Ile
CA2752217
NM_001114978.2:c.648G>C
CA2752218
NM_001114978.2:c.648G>A
CA355753349
NM_001114978.2:c.648G>T