Canonical Allele Identifier: PA174052
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 132926
ClinVar RCV Id: RCV000148975
ClinVar Variation Id: 578571
ClinVar RCV Id: RCV000701623
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe510Leu
CA010890
NM_000257.4:c.1530C>A
CA389050388
NM_000257.4:c.1530C>G
CA389050393
NM_000257.4:c.1528T>C