Canonical Allele Identifier: PA132127
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43097
ClinVar RCV Id: RCV000035992 RCV000767174 RCV004018783 RCV001727522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val236Ala
CA016653
NM_000257.4:c.707T>C