Canonical Allele Identifier: PA296680
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181262
ClinVar RCV Id: RCV000158666 RCV000628848 RCV000766461 RCV000778009 RCV002326904 RCV002492626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1560Gln
CA015224
NM_000257.4:c.4679G>A