ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829600910
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.179696407
Score
-0.1970860238
Score
-0.3143629794
Score
-0.1644897512
Linked Data - NCBI & NCI
ClinVar Allele:
994569
ClinVar RCV:
RCV001307584
ClinVar Variation:
1010014
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Phe90Ser
CA378924377
NM_005343.4:c.269T>C