Canonical Allele Identifier: PA2826927083
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_001295071.1:p.Asn904Thr
CA278928159
NM_001308142.2:c.2711A>C