Canonical Allele Identifier: PA296860
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181365
ClinVar RCV Id: RCV000158833 RCV003586158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1397del
CA014612
NM_000257.4:c.4190_4192del