Canonical Allele Identifier: PA2499230289
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016191
ClinVar RCV Id: RCV001315160 RCV004005081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1678His
CA045048
NM_000257.4:c.5032A>C