Canonical Allele Identifier: PA261357
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42934
ClinVar RCV Id: RCV000158830 RCV000707732
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu931del
CA013089
NM_000257.4:c.2791_2793del