Canonical Allele Identifier: PA1139682291
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 921354
ClinVar RCV Id: RCV001180707 RCV001875997
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035203.1:p.Arg1926His
CA394846333
NM_001040114.2:c.5777G>A