Canonical Allele Identifier: PA098120
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14121
ClinVar RCV Id: RCV000015178 RCV000156689 RCV000766473 RCV001068554 RCV002482868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1883Lys
CA016328
NM_000257.4:c.5647G>A