Canonical Allele Identifier: PA658805435
Gene: MAP2K1 HGNC NCBI

Linked Data

ClinVar Variation Id: 503540
ClinVar RCV Id: RCV000591643 RCV003767412
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002746.1:p.Leu313Phe
CA392937558
NM_002755.4:c.939G>C
CA392937559
NM_002755.4:c.939G>T