Canonical Allele Identifier: PA277669
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 217461
ClinVar RCV Id: RCV000201468 RCV000554994 RCV000777755 RCV004541282 RCV003133174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn1664Lys
CA044638
NM_000257.4:c.4992C>A
CA389037182
NM_000257.4:c.4992C>G