Canonical Allele Identifier: PA2573062042
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1321086
ClinVar RCV Id: RCV001777065
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys918Glu
CA389047179
NM_000257.4:c.2752A>G