ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829601087
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1980666988
Score
-0.0315881363
Score
0.136310994
Score
0.3043440172
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000595459
RCV000681102
RCV000700035
ClinVar Variation:
503536
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Arg149Trp
CA378922736
NM_005343.4:c.445C>T