Allele Registry

Canonical Allele Identifier: PA2829396969

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000030296

RCV000641574

RCV001753433

RCV002313723

RCV002496467

ClinVar Variation:

36618

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Ile1078Thr	CA214156 NM_002474.3:c.3233T>C