Canonical Allele Identifier: PA645414497
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 228909
ClinVar RCV Id: RCV001062631 RCV001191614 RCV003233499 RCV002354609
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala13Thr
CA038963
NM_000257.4:c.37G>A