Canonical Allele Identifier: PA645389625
Gene: MYH8 HGNC NCBI

Linked Data

ClinVar Variation Id: 321646
ClinVar RCV Id: RCV000300494 RCV000964359
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002463.2:p.Glu577Asp
CA8387988
NM_002472.3:c.1731G>C
CA398123099
NM_002472.3:c.1731G>T