Canonical Allele Identifier: PA915970030
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 659397
ClinVar RCV Id: RCV000816398 RCV004028886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Ile379Val
CA7624169
NM_002755.4:c.1135A>G