Canonical Allele Identifier: PA916006582
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376631
ClinVar RCV Id: RCV000420444 RCV000423328 RCV000423948 RCV000429869 RCV000430499 RCV000435486 RCV000440112 RCV000441661 RCV003509528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu72Arg
CA16603050
NM_001276761.3:c.215T>G