Canonical Allele Identifier: PA2828166431
Gene: MRTFB HGNC NCBI

Linked Data

ClinVar Variation Id: 2515301
ClinVar RCV Id: RCV004293869

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352341.1:p.Gly445Cys
CA7911329
NM_001365412.2:c.1333G>T