Allele Registry

Canonical Allele Identifier: PA1139678446

Gene: TP53 HGNC NCBI

ClinVar Variation Id: 919322

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119589.1:p.Met37Ile	CA397841683 NM_001126117.1:c.111G>C CA397841691 NM_001126117.1:c.111G>A CA397841695 NM_001126117.1:c.111G>T