Canonical Allele Identifier: PA1139675091
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 922222
ClinVar RCV Id: RCV001182154 RCV002327438 RCV002068308 RCV002466627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1596Leu
CA043848
NM_000257.4:c.4787C>T