Canonical Allele Identifier: PA180949
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177891
ClinVar RCV Id: RCV000154543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1899Ala
CA016376
NM_000257.4:c.5696T>C