Canonical Allele Identifier: PA2499230278
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023364
ClinVar RCV Id: RCV001323393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1436Asp
CA389040154
NM_000257.4:c.4306A>G