Canonical Allele Identifier: PA915956555
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 636588
ClinVar RCV Id: RCV000788458 RCV004027369
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp218Tyr
CA389052328
NM_000257.4:c.652G>T