Canonical Allele Identifier: PA645416937
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 374964
ClinVar RCV Id: RCV000415721 RCV000415697 RCV001180329 RCV001357744 RCV001865310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1289Trp
CA16043997
NM_000257.4:c.3865C>T