ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829600810
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.6647674349
Score
-0.3746097226
Score
-0.188826798
Score
-0.6526643336
Linked Data - NCBI & NCI
ClinVar Allele:
1709539
ClinVar RCV:
RCV002292422
ClinVar Variation:
1711128
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Asp57Ala
CA378924693
NM_005343.4:c.170A>C