Canonical Allele Identifier: PA2829399258
Gene: MYH11 HGNC NCBI

Linked Data

ClinVar Variation Id: 487586
ClinVar RCV Id: RCV000656148 RCV001176897
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002465.1:p.Asn1966Ser
CA394843490
NM_002474.3:c.5897A>G