Canonical Allele Identifier: PA658670633
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 479035
ClinVar RCV Id: RCV000806156 RCV000565488 RCV003459273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met2667Leu
CA382561792
NM_000051.4:c.7999A>C
CA382561793
NM_000051.4:c.7999A>T