Canonical Allele Identifier: PA296563
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181199
ClinVar RCV Id: RCV000158561 RCV001850215
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala899Glu
CA012871
NM_000257.4:c.2696C>A