Canonical Allele Identifier: PA645485934
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 375876
ClinVar RCV Id: RCV000417850 RCV000423218 RCV000425977 RCV000432522 RCV000430805 RCV000435607 RCV000436237 RCV000437557 RCV000445025 RCV004022195 RCV000424444 RCV000444067
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002515.1:p.Gly13Val
CA16602363
NM_002524.5:c.38G>T
CA645537999
NM_002524.5:c.38_39delinsTC