Canonical Allele Identifier: PA296690
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181268
ClinVar RCV Id: RCV000158674 RCV000473596
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1619Lys
CA015416
NM_000257.4:c.4855G>A