ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA256491
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.0339973553
Score
0.4471336794
Score
0.2778171375
Score
0.0147005349
Linked Data - NCBI & NCI
ClinVar Allele:
27644
ClinVar RCV:
RCV000013439
RCV000353386
ClinVar Variation:
12605
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Lys117Arg
CA256490
NM_005343.4:c.350A>G