Canonical Allele Identifier: PA2829995671
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 405477
ClinVar RCV Id: RCV000474612 RCV003441866
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.His683Gln
CA16614671
NM_022844.3:c.2049C>A
CA394868773
NM_022844.3:c.2049C>G