Canonical Allele Identifier: PA2826094506
Gene: MAP7D3 HGNC NCBI
ClinVar RCV:
RCV000972142
ClinVar Variation:
789502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166988.1:p.Arg116Gln
CA10525738
NM_001173517.2:c.347G>A