Canonical Allele Identifier: PA913194190
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 629778
ClinVar RCV Id: RCV000774490 RCV003748279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1023Val
CA035427
NM_000257.4:c.3068C>T