Canonical Allele Identifier: PA2826559156
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492752
ClinVar RCV Id: RCV000582529 RCV001055662
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ser67Arg
CA397844688
NM_001276695.3:c.201C>G
CA397844691
NM_001276695.3:c.201C>A
CA397844720
NM_001276695.3:c.199A>C