Canonical Allele Identifier: PA2829756359
Gene: MRTFB HGNC NCBI
ClinVar RCV:
RCV004500651
ClinVar Variation:
3210227
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054767.3:p.Ala772Thr
CA7911589
NM_014048.4:c.2314G>A