Canonical Allele Identifier: PA279317
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 217462
ClinVar RCV Id: RCV000201496 RCV001297501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn885Lys
CA279315
NM_000257.4:c.2655T>A
CA389047871
NM_000257.4:c.2655T>G