Canonical Allele Identifier: PA2828166576
Gene: MRTFB HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352342.1:p.Ala751Thr
CA7911589
NM_001365413.2:c.2251G>A