Canonical Allele Identifier: PA2829756317
Gene: MRTFB HGNC NCBI

Linked Data

ClinVar Variation Id: 3210133
ClinVar RCV Id: RCV004500557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054767.3:p.Asp364Gly
CA7911268
NM_014048.4:c.1091A>G