Canonical Allele Identifier: PA131892
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42937
ClinVar RCV Id: RCV000035830 RCV000656920 RCV000770486 RCV001362171 RCV004017297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu949Val
CA013153
NM_000257.4:c.2846A>T