Canonical Allele Identifier: PA2829395795
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072191
ClinVar RCV Id: RCV004012221
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Ser641Gly
CA394869122
NM_002474.3:c.1921A>G