Canonical Allele Identifier: PA1139673398
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 926111
ClinVar RCV Id: RCV001188502
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn885Tyr
CA389047877
NM_000257.4:c.2653A>T