Canonical Allele Identifier: PA131881
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42929
ClinVar RCV Id: RCV000035821
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile909Val
CA012966
NM_000257.4:c.2725A>G