Canonical Allele Identifier: PA2825111838
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2763277
ClinVar RCV Id: RCV003587925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu908Met
CA389047272
NM_000257.4:c.2722C>A