Canonical Allele Identifier: PA2825615928
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376646
ClinVar RCV Id: RCV000417607 RCV000420265 RCV000422133 RCV000424797 RCV000426301 RCV000427682 RCV000428293 RCV000433513 RCV000433712 RCV000435517 RCV000437485 RCV000443564 RCV000444453 RCV000633329 RCV001017582 RCV002289531
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Pro146His
CA16603063
NM_001126117.1:c.437C>A