Canonical Allele Identifier: PA344665
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42941
ClinVar RCV Id: RCV000035834 RCV000148698 RCV000199809 RCV000292823 RCV000334844 RCV000352353 RCV000725743 RCV000758042 RCV000845384 RCV001094109 RCV002490487 RCV002433495 RCV003320058 RCV004534741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met982Thr
CA013227
NM_000257.4:c.2945T>C