Canonical Allele Identifier: PA296738
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181293
ClinVar RCV Id: RCV000158720 RCV001525375 RCV001366152 RCV004019920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly10Ala
CA013294
NM_000257.4:c.29G>C