Canonical Allele Identifier: PA358297
Gene: TP53 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Ser127Cys
CA349567
NM_000546.6:c.380C>G