Canonical Allele Identifier: PA2829998507
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3070719
ClinVar RCV Id: RCV004013229
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_074035.1:p.Lys1849Asn
CA394847448
NM_022844.3:c.5547G>T
CA394847449
NM_022844.3:c.5547G>C