Canonical Allele Identifier: PA1139673697
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 915535
ClinVar RCV Id: RCV001170268
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1006Thr
CA389045889
NM_000257.4:c.3016G>A