Canonical Allele Identifier: PA2573062022
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1329414
ClinVar RCV Id: RCV001799457
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1682His
CA389037073
NM_000257.4:c.5046G>C
CA389037074
NM_000257.4:c.5046G>T