Canonical Allele Identifier: PA199007
Gene: MYH7 HGNC NCBI
ClinVar RCV:
RCV001170480
ClinVar Variation:
188648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1924Ile
CA016469
NM_000257.4:c.5771G>T