Canonical Allele Identifier: PA099029
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2578711
ClinVar RCV Id: RCV003326887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1044Ala
CA389045432
NM_000257.4:c.3131T>C