Canonical Allele Identifier: PA2828166684
Gene: MRTFB HGNC NCBI
ClinVar RCV:
RCV004500651
ClinVar Variation:
3210227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352343.1:p.Ala701Thr
CA7911589
NM_001365414.2:c.2101G>A