Canonical Allele Identifier: PA2828166514
Gene: MRTFB HGNC NCBI

Linked Data

ClinVar Variation Id: 3210133
ClinVar RCV Id: RCV004500557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352342.1:p.Asp293Gly
CA7911268
NM_001365413.2:c.878A>G