Canonical Allele Identifier: PA2828166370
Gene: MRTFB HGNC NCBI

Linked Data

ClinVar Variation Id: 3210249
ClinVar RCV Id: RCV004500673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352340.1:p.Asn893Thr
CA278928159
NM_001365411.2:c.2678A>C