Canonical Allele Identifier: PA131726
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42828
ClinVar RCV Id: RCV000035704 RCV000700699 RCV000769461 RCV002292459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp394Asn
CA010330
NM_000257.4:c.1180G>A