Canonical Allele Identifier: PA2829756367
Gene: MRTFB HGNC NCBI

Linked Data

ClinVar Variation Id: 3210249
ClinVar RCV Id: RCV004500673

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054767.3:p.Asn854Thr
CA278928159
NM_014048.4:c.2561A>C