Canonical Allele Identifier: PA097853
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 36641
ClinVar RCV Id: RCV000035878 RCV000030319 RCV000254007 RCV000588247 RCV000758038 RCV000765159 RCV000852700 RCV001112662 RCV001080835 RCV001112663 RCV003320036 RCV004532424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1327Lys
CA014310
NM_000257.4:c.3981C>A
CA389041322
NM_000257.4:c.3981C>G