Canonical Allele Identifier: PA1139673630
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 935528
ClinVar RCV Id: RCV001204141 RCV004010635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala970Val
CA257818867
NM_000257.4:c.2909C>T