Allele Registry

Canonical Allele Identifier: PA214169

Gene: MYH11 HGNC NCBI

ClinVar RCV:

RCV000182562

RCV000554857

RCV000611869

RCV000659924

RCV000762209

RCV002482921

ClinVar Variation:

36622

HGVS (amino-acid)	Matching Registered Transcripts
NP_002465.1:p.Lys1621Gln	CA214168 NM_002474.3:c.4861A>C