Canonical Allele Identifier: PA2579931429
Gene: HRAS HGNC NCBI
ClinVar RCV:
RCV000228331
ClinVar Variation:
240136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.His166Gln
CA10582922
NM_001130442.3:c.498C>A
CA378921136
NM_001130442.3:c.498C>G