Canonical Allele Identifier: PA167804
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 142224
ClinVar RCV Id: RCV000131223 RCV000203692 RCV000587634 RCV001530924 RCV003467169 RCV004551262
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Asn619His
CA167802
NM_000051.4:c.1855A>C