Canonical Allele Identifier: PA2826927043
Gene: MRTFB HGNC NCBI

Linked Data

ClinVar Variation Id: 3210133
ClinVar RCV Id: RCV004500557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295071.1:p.Asp364Gly
CA7911268
NM_001308142.2:c.1091A>G