Canonical Allele Identifier: PA2829395782
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 919619
ClinVar RCV Id: RCV001177898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Glu636Asp
CA394869146
NM_002474.3:c.1908G>T
CA394869147
NM_002474.3:c.1908G>C