Canonical Allele Identifier: PA296582
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181209
ClinVar RCV Id: RCV000158582 RCV001065622 RCV001187172 RCV002478479 RCV002433703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1004Glu
CA013300
NM_000257.4:c.3010C>G