Canonical Allele Identifier: PA645416589
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 432848
ClinVar RCV Id: RCV000497844 RCV001188967 RCV001290546 RCV001851383 RCV002438210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala970Thr
CA389046624
NM_000257.4:c.2908G>A