Canonical Allele Identifier: PA645506779
Gene: MAP3K7 HGNC NCBI

Linked Data

ClinVar Variation Id: 264698
ClinVar RCV Id: RCV000254565 RCV001530168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_663304.1:p.Pro512Leu
CA10588006
NM_145331.3:c.1535C>T