Canonical Allele Identifier: PA132049
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43047
ClinVar RCV Id: RCV000584779 RCV000694818 RCV000766465 RCV000769441 RCV003298058 RCV002490490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1652Tyr
CA015501
NM_000257.4:c.4954G>T