Canonical Allele Identifier: PA1139673558
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 946399
ClinVar RCV Id: RCV001217261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu926Val
CA034272
NM_000257.4:c.2776C>G