Canonical Allele Identifier: PA915993280
Gene: MAP7D3 HGNC NCBI
ClinVar RCV:
RCV000972142
ClinVar Variation:
789502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166987.1:p.Arg98Gln
CA10525738
NM_001173516.1:c.293G>A