Canonical Allele Identifier: PA645416607
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 432796
ClinVar RCV Id: RCV000498027 RCV001183003 RCV001857022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1007Val
CA389045880
NM_000257.4:c.3019C>G