Canonical Allele Identifier: PA658804485
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 520381
ClinVar RCV Id: RCV000620973 RCV000703483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys912Asn
CA389047222
NM_000257.4:c.2736G>T
CA389047224
NM_000257.4:c.2736G>C