ClinGen Allele Registry
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Canonical Allele Identifier:
PA645423148
Gene: MAP2K1
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000421374
RCV000431446
RCV000432046
RCV000442281
ClinVar Variation:
376447
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_002746.1:p.Phe53Ile
CA16602882
NM_002755.4:c.157T>A