Canonical Allele Identifier: PA645416578
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 264501
ClinVar RCV Id: RCV000249682 RCV000497921 RCV001859467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu961Arg
CA10587769
NM_000257.4:c.2882T>G