Canonical Allele Identifier: PA645389608
Gene: MYH8 HGNC NCBI

Linked Data

ClinVar Variation Id: 321655
ClinVar RCV Id: RCV000279822 RCV000502525 RCV000966459
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002463.2:p.Arg193His
CA8388313
NM_002472.3:c.578G>A